Zika Virus Inhibitors Based on a 1,3-Disubstituted 1H-Pyrazolo[3,4-d]pyrimidine-amine Scaffold

Abstract

To search for Zika virus (ZIKV) antivirals, we have further explored previously reported 7H-pyrrolo[2,3-d]pyrimidines by examining an alternative substitution pattern of their central scaffold, leading to compound 5 with low micromolar antiviral activity. To circumvent the synthetic difficulties associated with compound 5, we have exploited a 1H-pyrazolo[3,4-d]pyrimidine scaffold and performed structure-activity relationship studies on its peripheral rings A and B. While ring B is less sensitive to structural modifications, an electron-withdrawing group at the para position of ring A is preferred for enhanced antiviral activity. Overall, we have not only discovered an alternative substitution pattern centered on a 1H-pyrazolo[3,4-d]pyrimidine scaffold but also generated anti-ZIKV compounds including 6 and 13, which possess low micromolar antiviral activity and relatively low cytotoxicity. These compounds represent new chemotypes that will be further optimized in our continued efforts to discover anti-ZIKV agents.

1. Introduction

Zika virus (ZIKV) was first isolated in and named after the Zika forest of Uganda in 1947 [1]. The first human cases of ZIKV infection were reported in 1952 in the United Republic of Tanzania and Uganda, followed by outbreaks on the Yap Islands in Micronesia in 2007 and French Polynesia in 2013 [2]. However, it was the 2015–2016 global epidemic that attracted public attention and led to the declaration of ZIKV as a global public health emergency by the World Health Organization (WHO) in 2016 [3]. This declaration was in part due to the finding that ZIKV infection was associated with devastating neurological disorders, including congenital microcephaly in newborn infants and Guillain-Barré syndrome in adults [4]. As of December 2021, 89 countries have reported local transmission but currently no outbreaks have been reported [5]. Because the virus is still circulating in these areas and there is an increase in the mosquito-circulating areas due to overpopulation and urbanization, the risk for a new Zika virus is still relevant.

ZIKV is a member of the genus Flavivirus, which also includes important mosquito-borne viruses such as dengue virus (DENV), West Nile virus (WNV), yellow fever virus (YFV), and Japanese encephalitis virus (JEV) [6]. Like other Flavivirus members, ZIKV virions contain a single-stranded, positive-sense genomic RNA, which is translated into a single polyprotein and subsequently processed to give three structural proteins (capsid (C), pre-membrane/membrane (prM/M), and envelope(E)) and seven nonstructural (NS) proteins (NS1, NS2A, NS2B, NS3, NS4A, NS4B, and NS5) [7]. These ZIKV proteins, especially NS2B-NS3 [8] and NS5 [9], have been actively explored as direct-acting antiviral targets in efforts to discover anti-ZIKV agents [10,11,12]. Furthermore, phenotypic screening of commercially available or in-house compound libraries has also been pursued as an alternative strategy [13]; however, identifying the molecular target of screening hits remains a challenging task and further hit-to-lead optimization requires significant medicinal chemistry efforts. Moreover, repurposing advanced small molecules, especially those that have been fully evaluated in clinical trials, is an effective approach to identifying ZIKV antivirals [14,15,16].

In our initial efforts to identify anti-ZIKV agents, we have discovered several inhibitors including compound 1 (Figure 1) that display promising anti-ZIKV activity, especially in the gold standard titer-reduction assay [17]. We have also demonstrated that compound 1’s 7H-pyrrolo[2,3-d]pyrimidine scaffold can be replaced by 9H-purine or 1H-pyrazolo[3,4-d]pyrimidine as shown in compounds 2 and 3, respectively. These compounds feature a substitution pattern as exemplified by the one in 4,7-disubstituted 7H-pyrrolo[2,3-d]pyrimidine 1. To search for new anti-ZIKV chemotypes, we have examined alternative substitution patterns built on previously reported 7H-pyrrolo[2,3-d]pyrimidine and 1H-pyrazolo[3,4-d]pyrimidine central scaffolds. Here we report the structure-activity relationship (SAR) studies and highlight structural features that contribute to antiviral activity.

2. Results and Discussion

In the current study, we continued to use our previously reported luciferase-based ZIKV reporter assay as a primary antiviral screening, by which newly synthesized compounds were tested (at 10 µM) along with NITD008 (Figure 1, at 1 µM) [18], a flavivirus RNA-dependent RNA polymerase (RdRp) inhibitor, and NSC 12155 (Figure 1, at 10 µM) [19], a flavivirus NS5 methyltransferase (MTase) inhibitor, as reference compounds (

Table 1. SAR study on the scaffold replacement.

Compd	X	ZIKV Reporter Assay			Titer Reduction Assay		CC50 (µM)
		Inhibition (%) at 10 µM	Viability (%) at 10 µM	EC50 (µM)	% at 8.5 µM	EC50 (µM)
4	NH	91	40
5	O	62	82		94	4.3	58
DMSO		0	100		0
NITD008 (1 µM) a		100	100	0.14	100 (ND b)		>45
NSC 12155 a		68	70	2.18	72	7.34	23.0

^a Reported previously [17]; ^b ND, no plaque detected.

). Inhibitors that showed good anti-ZIKV activity and relatively low cytotoxicity in the reporter assay were tested in the gold standard titer reduction assay at 8.5 µM. For active compounds (>60% titer-reduction), dose-response experiments were performed to determine EC₅₀ (half maximal effective concentration, a concentration that is needed to cause half of the maximum possible pharmacological effect) and CC₅₀ (half cytotoxic concentration, a concentration that is required to reduce cell viability by 50%) values. For selected compounds, EC₅₀ values in the reporter assay were also measured.

We first examined compounds 4 and 5, in which a 7H-pyrrolo[2,3-d]pyrimidine core structure was retained with an altered substitution pattern (Figure 1). In both compounds, a substituent was placed at position 5 in contrast to position 4 in compound 1. Furthermore, instead of the benzyl amine functionality in compound 1, a methylamino and methoxy linkage was used in compounds 4 and 5, respectively. When tested at 10 µM in the reporter assay, compound 4 showed excellent antiviral activity (Table 1), which unfortunately could be due to its high intrinsic toxicity. In comparison, compound 5 was significantly less toxic and possessed good anti-ZIKV activity in the reporter assay. Compound 5’s excellent antiviral activity (94% reduction at 8.5 µM) was revealed in the titer reduction assay and its EC₅₀ (titer reduction) and CC₅₀ values were further determined as 4.3 µM and 58 µM, respectively (Table 1). Given the fact that compound 1 had EC₅₀ and CC₅₀ values of 5.2 µM and 20 µM, respectively, compound 5 possessed comparable antiviral activity and was significantly less toxic. These results suggested that compound 5 represented a new, promising substitution pattern built on the 7H-pyrrolo[2,3-d]pyrimidine scaffold and warranted further SAR studies.

Unfortunately, the synthesis of compound 5 proved to be extremely difficult most likely due to an intrinsic elimination reaction of activated intermediate 39 (see discussion below and Scheme 1). To facilitate SAR studies, we chose to investigate compound 6 and its analogs (Figure 1), which were based on 1H-pyrazolo[3,4-d]pyrimidine, a chemical type that was expected to circumvent the elimination reaction encountered during the synthesis of compound 5. Compound 6 also had a substitution pattern identical to that of compound 5, featuring two substituents at positions 1 and 3 of 1H-pyrazolo[3,4-d]pyrimidine, respectively (Figure 1). When tested in the reporter virus assay, compound 6 displayed anti-ZIKV and cytotoxicity at levels almost identical to those of compound 5 (

Table 2. SAR study on ring A of 1H-pyrazolo[3,4-d]pyrimidin-4-amine analogs.

Compd	A	ZIKV Reporter Assay			Titer Reduction Assay		CC50 (µM)
		Inhibition (%) at 10 µM	Viability (%) at 10 µM	EC50 (µM)	% at 8.5 µM	EC50 (µM)
6		65	82		65	5.1	39
7		0	99
8		9	103
9		90	37
10		0	99
11		0	89
12		0	95
13		68	86		73	6.5	>100
14		58	93		52
15		37	99
16		0	95
17		88	38
18		6	95
19		63	77		22
20		88	39
21		82	64	3.5	74	5.2	25
22		67	36
23		49	82		20
24		62	36
25		68	40

). Moreover, it had EC₅₀ (titer reduction) and CC₅₀ values of 5.1 µM and 39 µM, respectively. The fact that compounds 5 and 6 possessed similar antiviral activity and cytotoxicity in both assays clearly indicated that 1H-pyrazolo[3,4-d]pyrimidine could indeed serve as an alternative scaffold. Therefore, we decided to focus on compound 6 analogs, which were synthetically more accessible and proceeded to explore the substituents at positions 1 and 3.

At position 1, compound 6 contained a phenyl ring (ring A), where a nitro group was attached at the para position. As our initial efforts, we prepared compound 7 with no substituents on ring A (Table 2). While compound 7 was not toxic, its anti-ZIKV activity was also abolished. This result suggested that a substituent at the para position was crucial to anti-ZIKV activity. To examine the effect of the modification site, we prepared compounds 8 and 9, which had a nitro group at the ortho and meta position, respectively. Like compound 7, compound 8 also lost its anti-ZIKV activity, eliminating the ortho position as a viable modification site. On the other hand, while compound 9 exhibited enhanced anti-ZIKV activity, its high cytotoxicity suggested that the meta position was not an ideal modification site. Since the nitro group was an electron-withdrawing group, we proceeded to prepare compounds 10–12, in which the nitro group was reduced to the corresponding electron-donating aniline group (Table 2). None of these compounds displayed observable anti-ZIKV activity in the reporter assay, suggesting an electron-withdrawing group was preferred for antiviral activity. Taken together, these results demonstrated that an electron-withdrawing group at the para position of ring A was highly desirable.

Accordingly, we continued to investigate additional electron-withdrawing groups by preparing compounds 13–15, in which trifluoromethyl, methylsulfonyl, and cyano, respectively, were placed at the para position of ring A (Table 2). Compound 13 showed anti-ZIKV activity and cytotoxicity at levels very similar to those of compound 6 in the reporter assay, suggesting that trifluoromethyl is also a productive substituent. This finding was further supported by compound 13’s good antiviral activity (EC₅₀ = 6.5 µM) in the titer reduction assay. In comparison, compounds 14 and 15 exhibited relatively lower anti-ZIKV activity. Nonetheless, their significant anti-ZIKV activity confirmed the beneficial effect of a para-positioned electron-withdrawing group when compared with non-substituted compound 7. Taken together, these results showed that other electron-withdrawing groups such as trifluoromethyl could be used to enhance antiviral activity.

Encouraged by the above finding, we decided to explore methyl ester (Table 2), a functional group that was electron-withdrawing and, if necessary, could be further converted into other derivatives. When a methyl ester was placed at the ortho position, the resulting compound 16 had no anti-ZIKV activity in the reporter assay, indicating that modifications at this position had a detrimental effect. Compound 17, which contained a meta-positioned methyl ester, had excellent anti-ZIKV activity; however, such activity was accompanied by high cytotoxicity. These SAR trends were in line with those observed when a nitro group was examined in compounds 8 and 9. Surprisingly, compound 18, in which a methyl ester was placed at the para position, had minimal anti-ZIKV activity, a SAR trend that clearly contradicted that seen in compounds 6 vs. 7. This finding suggested that an increased steric effect imposed by a methyl ester group was not tolerated at the para position. To examine the steric effect, methyl ester 18 was converted into the corresponding primary amide 19, a transformation that restored anti-ZIKV activity and cytotoxicity to levels similar to those of compound 6. Unfortunately, compound 19 exhibited low antiviral activity in the titer reduction assay, an observation for further investigation in the future.

We next investigated whether the phenyl ring in compound 6 and its analogs could be replaced by a pyridine ring by taking advantage of the latter’s electron-deficient nature (Table 2). We first synthesized compounds 20 and 21, in which an electron-withdrawing chloro group was attached at the meta and para position, respectively. Both compounds showed good anti-ZIKV activity in the reporter assay even though compound 21 was less toxic than 20. The finding generally mirrored the SAR trend observed in compounds 6 vs. 9. When tested in the titer reduction assay, while compound 21 possessed antiviral activity (EC₅₀ = 5.2 µM) almost identical to that of compound 6, it showed enhanced cytotoxicity (CC₅₀ = 25 µM). We also explored the electron-donating amino group, which was placed at the meta and para position, leading to compounds 22 and 23, respectively. Both compounds still retained significant anti-ZIKV activity. This finding contradicted the one seen in compounds 11 and 12, where an amino group abolished anti-ZIKV activity. We also evaluated synthetic intermediates 24 and 25, which displayed no drastic change in anti-ZIKV activity or cytotoxicity in comparison with compounds 22 and 23, respectively. Taken together, these results suggested that a pyridine ring could be used to replace the phenyl ring in compound 6; however, such isosteric change might lead to different SAR trends, which warrant future investigation.

After examining ring A, we continued to investigate the effect of substitution on ring B (

Table 3. SAR study on ring B of 1H-pyrazolo[3,4-d]pyrimidin-4-amine analogs.

Compd	R	A	ZIKV Reporter Assay			Titer Reduction Assay		CC50 (µM)
			Inhibition (%) at 10 µM	Viability (%) at 10 µM	EC50 (µM)	% at 8.5 µM	EC50 (µM)
26	o-Me		60	77
27	m-Me		71	82		53
28	p-Me		65	85		34
29	o-Cl		34	94
30	m-Cl		52	93		11
31	p-Cl		60	94		40

). To that end, a para-NO₂ substituted phenyl ring A was retained and an electron-donating methyl group was introduced at different positions of ring B, giving rise to compounds 26–28. These compounds displayed anti-ZIKV activity and cytotoxicity comparable to those of compound 6, suggesting that an electron-donating methyl group exerted minimal effect regardless of the substitution pattern. When an electron-withdrawing chloro group was attached at different positions of ring B, the resulting compounds 29–31 exhibited lower anti-ZIKV activity in comparison with compound 6, pointing to chloro group’s having a negative effect. Taken together, these findings suggested that ring B was less sensitive to structural modifications. Given that methyl and chloro groups were relatively simple, substituents or functional groups that would elicit additional interactions, such as hydrogen bonds, could be candidates for future SAR investigation of ring B.

The syntheses of 5,7-disubstituted 7H-pyrrolo[2,3-d]pyrimidin-4-amines 4 and 5 were depicted in Scheme 1. Bromination of commercially available 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (32) was performed by following literature procedures to give bromide 33 [20]. The introduction of a formyl group at position 5 was accomplished by halogen-metal exchange at −78 °C followed by treatment with dimethylformamide (DMF), giving rise to aldehyde 34 in excellent yields. Subsequent alkylation with 4-nitrobenzyl bromide gave aldehyde 35, which was reduced to the corresponding alcohol 36. Reductive amination reaction of aldehyde intermediate 35 and aniline afforded chloride 37, which was subsequently subjected to aminolysis at high temperature to give compound 4 in 18% yield. To prepare compound 5, alcohol intermediate 36 was initially activated through the formation of a chloride or mesylate followed by a nucleophilic attack; Unfortunately, these synthetic methods failed most likely because of an activated intermediate (generally represented by 39) that readily underwent elimination reaction to generate an unstable, unproductive intermediate 40. Alternatively, the Mitsunobu reaction of alcohol 36 and phenol gave rise to a complex reaction mixture most likely due to an oxyphosphonium intermediate 39, which was also susceptible to elimination reaction. Nonetheless, when the mixture was subjected to aminolysis without further purification, compound 5 was obtained with a very low combined yield.

Since the synthesis of compound 5 was extremely difficult, we focused on compounds featuring a 1H-pyrazolo[3,4-d]pyrimidine core structure, whose preparation was depicted in Scheme 2. Commercially available 3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (41) was first protected on the N1 position to give trityl 42, which was further modified on position 3. After the Stille coupling reaction, bromide 42 was converted into olefin 43, whose double bond was cleaved to form aldehyde 44 in excellent yields. Reduction of 44 gave alcohol 45, which was in turn used to prepare the key intermediate 46. Gratifyingly, when alcohol 45 was activated via a mesylate and subsequently replaced with different phenols, phenyl ether 46 was obtained in moderate to good yields without major side products. After the trityl group in 46 was removed, the resulting free N1 in 47 was alkylated with bromide 48 followed by additional transformations, if needed, to give compound 6–31 in a range of yields.

3. Conclusions

Expanding on our 7H-pyrrolo[2,3-d]pyrimidines ZIKV inhibitors, we have demonstrated that the central 7H-pyrrolo[2,3-d]pyrimidine scaffold can be donned with a different substitution pattern, giving rise to compound 5 as a low micromolar anti-ZIKV inhibitor. To circumvent the synthetic difficulties associated with compound 5, we have designed compounds based on a 1H-pyrazolo[3,4-d]pyrimidine scaffold as exemplified by compound 6. SAR studies of these compounds have revealed that an electron-withdrawing group at the para position of ring A is preferred for enhanced antiviral activity. Furthermore, it is feasible to replace the phenyl ring A in compound 6 with a pyridine ring without sacrificing antiviral activity. Nonetheless, we have also shown that relatively simple structural modifications on ring B have a minor impact on anti-ZIKV activity and cytotoxicity. Overall, we have discovered an alternative substitution pattern built on a 1H-pyrazolo[3,4-d]pyrimidine scaffold, leading to anti-ZIKV compounds including 6 and 13. These new compounds together with those based on 7H-pyrrolo[2,3-d]pyrimidines, 9H-purines, and 1H-pyrazolo[3,4-d]pyrimidines represent promising starting chemotypes to discover new anti-ZIKV agents.

4. Experimental Section

4.1. General Procedures

All commercial reagents were used as provided unless otherwise indicated. An anhydrous solvent dispensing system (J.C. Meyer) using 2 packed columns of neutral alumina was used for drying THF, Et₂O, and CH₂Cl_2, whereas 2 packed columns of molecular sieves were used to dry DMF. Solvents were dispensed under argon. Flash chromatography was performed with RediSep R_f silica gel columns on a Teledyne ISCO CombiFlash^® R_f system using the solvents as indicated. Nuclear magnetic resonance spectra were recorded on a Varian 600 MHz or Bruker 400 MHz spectrometer with Me₄Si or signals from the residual solvent as the internal standard for ¹H or ¹³C. Chemical shifts are reported in ppm, and signals are described as s (singlet), d (doublet), t (triplet), q (quartet), m (multiplet), br s (broad singlet), and dd (double doublet). Values given for coupling constants are first order. High-resolution mass spectra were recorded on an Agilent TOF II TOF/MS instrument equipped with either an ESI or APCI interface at the Center for Drug Design, University of Minnesota.

4.2. Chemistry

4.2.1. 5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine (33) [20]

To a solution of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (32, 2.51 g, 16.3 mmol) in anhydrous DMF (50 mL) was added NBS (2.91 g, 16.4 mmol) in anhydrous DMF (22 mL) in 25 min. The resulting mixture was stirred at rt for 1 h and poured into vigorously stirring water (350 mL). The precipitate was filtered, washed with water, suction-dried, and dried in vacuo to give compound 33 as a pale solid (3.55 g, 94%). ¹H NMR (600 MHz, DMSO-d₆) δ 13.00 (s, 1H), 8.63 (s, 1H), 7.96 (s, 1H). HRMS (ESI⁻) m/z calcd for C₆H₂BrClN₃ [M-H]⁻ 229.9126, found 229.9124.

4.2.2. 4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehyde (34)

ⁿBuLi (1.6 M in hexanes, 10.5 mL, 16.8 mmol) was added dropwise to a solution of 33 (1.78 g, 7.66 mmol) in anhydrous THF (80 L) at −78 °C. The resulting mixture was stirred at −78 °C for 1 h, and anhydrous DMF (0.66 mL, 8.5 mmol) was added dropwise. After the reaction mixture was stirred at −78 °C for 30 min and then at room temperature overnight, it was cooled at 0 °C and carefully quenched with water (40 mL). The mixture was concentrated to produce a thick syrup, which was treated with saturated NH₄Cl (60 mL) and vigorously stirred for 20 min. The solid that formed was filtered, washed with water (10 mL × 3), EtOAc (10 mL × 3), suction-dried, and dried in vacuo to give compound 34 as a pale solid (1.31 g, 94%). ¹H NMR (600 MHz, DMSO-d₆) δ 13.55 (s, 1H), 10.23 (s, 1H), 8.74 (s, 1H), 8.59 (s, 1H). HRMS (APCI⁺) m/z calcd for C₇H₅ClN₃O [M + H]⁺ 182.0116, found 182.0109.

4.2.3. 4-Chloro-7-(4-nitrobenzyl)-7H-nyrrolo[2,3-d]pyrimidine-5-carbaldehyde (35)

To a suspension of 34 (363 mg, 2.00 mmol) in anhydrous CH₃CN (20 mL), K₂CO₃ (829 mg, 6.00 mmol) and 4-nitrobenzyl bromide (561 mg, 2.60 mmol) were added. The resulting mixture was stirred at room temperature for 23 h and then poured into stirring water (100 mL). The precipitate was filtered, washed with water, and suction-dried. The solid was suspended in ether (10 mL) and the mixture was vigorously stirred for 30 min. After filtration, the solid was washed with ether and dried in vacuo to give compound 35 as a light-yellow solid (576 mg, 91%). ¹H NMR (600 MHz, CDCl₃) δ 10.50 (s, 1H), 8.78 (s, 1H), 8.22 (d, J = 8.7 Hz, 2H), 8.06 (s, 1H), 7.45 (d, J = 8.7 Hz, 2H), 5.62 (s, 2H). HRMS (APCI⁺) m/z calcd for C₁₄H₁₀ClN₄O₃ [M + H]⁺ 317.0436, found 317.0440.

4.2.4. 4-Chloro-7-(4-nitrobenzyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl)Methanol (36)

To a suspension of 35 (561 mg, 1.77 mmol) in THF (20 mL) and MeOH (20 mL) at 0 °C, NaBH₄ (420 mg, 11.1 mmol) was added in small portions. After the resulting mixture was stirred at 0 °C for 30 min, the reaction was carefully quenched with an NH₄Cl solution (30 mL of saturated NH₄Cl and 10 mL of water), and the mixture was extracted with CHCl₃ (40 × 2 mL). The combined organic layer was concentrated, and the residue was purified by flash column chromatography (0–10% MeOH/CH₂Cl₂) to give compound 36 as a yellow solid (473 mg, 84%). ¹H NMR (600 MHz, CDCl₃) δ 8.65 (s, 1H), 8.14 (d, J = 8.7 Hz, 2H), 7.37 (d, J = 8.7 Hz, 2H), 7.26 (s, 1H), 5.54 (s, 2H), 4.98 (s, 2H), 2.05 (s, 1H). HRMS (APCI⁺) m/z calcd for C₁₄H₁₂ClN₄O₃ [M + H]⁺ 319.0592, found 319.0587.

4.2.5. N-((4-Chloro-7-(4-nitrobenzyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl)pethyl)pniline (37)

To a suspension of 35 (120 mg, 0.379 mmol) in anhydrous dichloroethane (6 mL), aniline (42 µL, 0.46 mmol), Na(OAc)₃BH (241 mg, 1.14 mmol), and acetic acid (22 µL, 0.38 mmol) were added. The resulting mixture was stirred at room temperature for 40 h and diluted with CH₂Cl₂ (20 mL). The organic layer was washed with saturated NaHCO₃ (10 mL), water (10 mL), and brine (20 mL). After concentration, the residue was purified by flash column chromatography (30–90% EtOAc/hexanes) to give compound 37 as a yellow solid (68 mg, 46%). ¹H NMR (600 MHz, CDCl₃) δ 8.64 (s, 1H), 8.15 (d, J = 8.7 Hz, 2H), 7.28 (d, J = 8.7 Hz, 2H), 7.19–7.16 (m, 3H), 6.74 (t, J = 7.2 Hz, 1H), 6.67–6.65 (m, 2H), 5.49 (s, 2H), 4.67 (s, 2H), 4.18 (s, 1H). HRMS (APCI⁺) m/z calcd for C₂₀H₁₇ClN₅O₂ [M + H]⁺ 394.1065, found 394.1060.

4.2.6. 7-(4-Nitrobenzyl)-5-((phenylamino)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine (4)

A solution of 37 (61 mg, 0.16 mmol) in dioxane (3 mL) and strong ammonia solution (3 mL) was heated at 120 °C for 6 h in a sealed tube and allowed to cool to room temperature. The mixture was concentrated, and the residue was purified by flash column chromatography (0–10% MeOH/CH₂Cl₂) to give compound 4 as a yellow solid (11 mg, 18%). ¹H NMR (600 MHz, CDCl₃) δ 8.32 (s, 1H), 8.18 (d, J = 8.7 Hz, 2H), 7.34 (d, J = 8.7 Hz, 2H), 7.28–7.26 (m, 2H), 6.91–6.89 (m, 2H), 6.84–6.82 (m, 2H), 6.08 (s, 2H), 5.46 (s, 2H), 4.35 (s, 2H), 3.85 (s, 1H). HRMS (ESI⁺) m/z calcd for C₂₀H₁₉N₆O₂ [M + H]⁺ 375.1564, found 375.1561.

4.2.7. 7-(4-Nitrobenzyl)-5-(phenoxymethyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine (5)

Phenol (58 mg, 0.62 mmol), Ph₃P (162 mg, 0.618 mmol), and then DEAD (97 µL, 0.62 mmol, dropwise) were added to a solution of 36 (131 mg, 0.411 mmol) in anhydrous THF (7 mL) at 0 °C. The resulting mixture was stirred at 0 °C for 1 h and then at room temperature for 20 h. After concentration, the residue was purified by flash column chromatography (10–90% EtOAc/hexanes) to give a white solid (121 mg), which contained a small amount of compound 38. The solid was dissolved in dioxane (5 mL) and strong ammonia solution (5 mL) in a sealed tube. The resulting mixture was heated at 120 °C for 6 h and allowed to cool to room temperature. After the mixture was concentrated, the residue was purified by preparative thin layer chromatography (5% MeOH/CH₂Cl₂) to give compound 5 as a yellowish solid (5 mg). ¹H NMR (600 MHz, CDCl₃/CD₃OD) δ 8.17 (d, J = 8.4 Hz, 2H), 8.11 (s, 1H), 7.38–7.36 (m, 1H), 7.30 (d, J = 8.4 Hz, 2H), 7.10–7.04 (m, 2H), 6.90–6.84 (m, 2H), 6.80 (t, J = 8.4 Hz, 1H), 5.45 (s, 2H), 4.10 (s, 2H). HRMS (ESI⁺) m/z calcd for C₂₀H₁₈N₅O₃ [M + H]⁺ 376.1404, found 376.1400.

4.2.8. 3-Bromo-1-trityl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (42)

Cs₂CO₃ (6.55 g, 20.1 mmol) and trityl chloride (2.94 g, 10.5 mmol) were added to a solution of 3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (41, 2.14 g, 10.0 mmol) in anhydrous DMF (50 mL). The resulting mixture was heated at 60 °C for 21 h, allowed to cool to room temperature, and poured into ice-water (300 mL). After the mixture was vigorously stirred for 30 min, the precipitate was filtered, washed with water, suction-dried, and dried in vacuo to give compound 42 as a white solid. (4.58 g, quantitative yield). ¹H NMR (600 MHz, CDCl₃) δ 8.05 (s, 1H), 7.32–7.21 (m, 15H), 5.91 (s, 2H). HRMS (ESI⁺) m/z calcd for C₂₄H₁₉BrN₅ [M + H]⁺ 456.0818, found 456.0811.

4.2.9. 1-Trityl-3-vinyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (43)

Pd(PPh₃)₄ (588 mg, 0.509 mmol) was added to a suspension of 42 (4.57 g, 10.0 mmol) in anhydrous toluene (100 mL). After the mixture was evacuated and backfilled with argon for three times, tributyl(vinyl)tin (3.51 mL, 12.0 mml) was added. The resulting mixture was heated at 110 °C for 6 h, allowed to cool to room temperature, diluted with EtOAc (200 mL), and treated with KF (7 g) for 15 min. After Celite was added, the mixture was stirred for 15 min and filtered. The filtrate was concentrated, and the residue was purified by flash column chromatography (20–100% EtOAc/hexanes) to give compound 43 as a yellowish solid (3.89 g, 96%). ¹H NMR (600 MHz, CDCl₃) δ 8.07 (s, 1H), 7.28–7.23 (m, 15H), 6.94 (dd, J = 17.8, 11.0 Hz, 1H), 5.90 (dd, J = 17.8, 1.3 Hz, 1H), 5.60–5.54 (m, 3H). HRMS (ESI⁺) m/z calcd for C₂₆H₂₂N₅ [M + H]⁺ 404.1870, found 404.1867.

4.2.10. 4-Amino-1-trityl-1H-pyrazolo[3,4-d]pyrimidine-3-carbaldehyde (44)

OsO₄ solution (2.5 wt% in ^tBuOH, 0.94 mL, 0.075 mmol) was added to a suspension of 43 (3.00 g, 7.44 mmol) in dioxane (120 mL) and water (40 mL). After the mixture was stirred at room temperature for 30 min, NaIO₄ (3.20 g, 15.0 mmol) was added. The resulting mixture was stirred for an additional 4 h, and dioxane was removed in vacuo. Water (60 mL) was added to the resulting slurry and the mixture was stirred for 15 min. The precipitate was filtered, washed with water, suction-dried, and dried in vacuo to give compound 44 as a pale solid (3.00 g, 99%). ¹H NMR (600 MHz, CDCl₃) δ 9.91 (s, 1H), 8.08 (s, 1H), 7.29–7.27 (m, 12H), 7.19–7.17 (m, 3H). HRMS (ESI⁻) m/z calcd for C₂₅H₁₈N₅O [M-H]⁻ 404.1517, found 404.1515.

4.2.11. 4-Amino-1-trityl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)methanol (45)

NaBH₄ (1.12 g, 29.6 mmol) was added in small portions to a solution of 44 (2.98 g, 7.35 mmol) in THF (50 mL) and MeOH (50 mL) at 0 °C. After the resulting mixture was stirred at 0 °C for 1 h, the reaction was carefully quenched with an NH₄Cl solution (100 mL of saturated NH₄Cl and 35 mL of water), and the mixture was extracted with CHCl₃ (200 mL). The organic layer was dried over Na₂SO₄ and filtered. The filtrate was concentrated, and the residue was purified by flash column chromatography (0–10% MeOH/CH₂Cl₂) to give compound 45 as a white fluffy solid (2.42 g, 81%). ¹H NMR (600 MHz, DMSO-d₆) δ 7.86 (s, 1H), 7.27–7.13 (m, 15H), 6.20 (t, J = 5.3 Hz, 1H), 4.67 (d, J = 5.3 Hz, 2H). HRMS (ESI⁺) m/z calcd for C₂₅H₂₂N₅O [M + H]⁺ 408.1819, found 408.1818.

4.2.12. 3-(Phenoxymethyl)-1-trityl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (46a)

Methanesulfonic anhydride (1.68 g, 9.64 mmol) was added to a suspension of 45 (3.29 g, 8.07 mmol), Et₃N (1.35 mL, 9.68 mmol), and DMAP (100 mg, 0.82 mmol) in CH₂Cl₂ (80 mL) at 0 °C. The resulting mixture was stirred at 0 °C for 1 h and diluted with CHCl₃ (240 mL). The organic layer was washed water (80 mL × 2) and brine (300 mL), and then concentrated to give a pale solid. The residue was immediately dissolved in anhydrous DMF (80 mL), then Cs₂CO₃ (7.90 g, 24.2 mmol) and phenol (1.60 g 17.0 mmol) were added. The resulting mixture was stirred at room temperature for 2 h, and DMF was removed in vacuo. The residue was partitioned between CHCl₃ (300 mL) and water (100 mL). The organic layer was washed with water (100 mL) and brine (200 mL) and dried over Na₂SO₄. After filtration, the filtrate was concentrated, and the residue was purified by flash column chromatography (30–100% EtOAc/hexanes) to give compound 46a as a pale solid (3.09 g, 79%). ¹H NMR (600 MHz, CDCl₃) δ 8.06 (s, 1H), 7.32–7.23 (m, 17H), 7.04–7.01 (m, 3H), 5.37 (s, 2H). No desired ionization observed in ESI or APCI modes.

4.2.13. 3-((o-Tolyloxy)methyl)-1-trityl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (46b)

Compound 46b was prepared from 45 (540 mg, 1.33 mmol) and o-cresol (289 mg, 2.67 mmol) as described for compound 46a. Pale solid, 447 mg, yield 68%. ¹H NMR (600 MHz, CDCl₃) δ 8.06 (s, 1H), 7.28–7.24 (m, 15H), 7.18–7.16 (m, 1H), 7.14 (td, J = 7.8, 1.4 Hz, 1H), 7.01–6.97 (m, 1H), 6.93 (td, J = 7.8, 1.2 Hz, 1H), 6.11 (s, 2H), 5.36 (s, 2H), 2.29 (s, 3H). No desired ionization was observed in ESI or APCI modes.

4.2.14. 3-((m-Tolyloxy)methyl)-1-trityl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (46c)

Compound 46c was prepared from 45 (540 mg, 1.33 mmol) and m-cresol (289 mg, 2.67 mmol) as described for compound 46a. Pale solid, 391 mg, yield 59%. ¹H NMR (600 MHz, CDCl₃) δ 8.06 (s, 1H), 7.28–7.23 (m, 15H), 7.19 (t, J = 7.8 Hz, 1H), 6.86–6.81 (m, 3H), 6.12 (s, 2H), 5.35 (s, 2H), 2.33 (s, 3H). No desired ionization was observed in ESI or APCI modes.

4.2.15. 3-((p-Tolyloxy)methyl)-1-trityl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (46d)

Compound 46d was prepared from 45 (540 mg, 1.33 mmol) and p-cresol (289 mg, 2.67 mmol) as described for compound 46a. White solid, 442 mg, yield 67%. ¹H NMR (600 MHz, CDCl₃) δ 8.05 (s, 1H), 7.28–7.24 (m, 15H), 7.10 (d, J = 8.5 Hz, 2H), 6.91 (d, J = 8.5 Hz, 2H), 6.13 (s, 2H), 5.33 (s, 2H), 2.31 (s, 3H). No desired ionization was observed in ESI or APCI modes.

4.2.16. 3-((2-Chlorophenoxy)methyl)-1-trityl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (46e)

Compound 46e was prepared from 45 as described for compound 46a. ¹H NMR (600 MHz, CDCl₃) δ 8.04 (s, 1H), 7.37 (dd, J = 7.9, 1.6 Hz, 1H), 7.25–7.21 (m, 15H), 7.16 (ddd, J = 8.9, 7.4, 1.6 Hz, 1H), 7.05 (dd, J = 8.4, 1.3 Hz, 1H), 6.94 (td, J = 7.7, 1.3 Hz, 1H), 6.13 (s, 2H), 5.44 (s, 2H). No desired ionization was observed in ESI or APCI modes.

4.2.17. 3-((3-Chlorophenoxy)methyl)-1-trityl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (46f)

Compound 46f was prepared from 45 as described for compound 46a. ¹H NMR (600 MHz, CDCl₃) δ 8.05 (s, 1H), 7.26–7.22 (m, 15H), 7.19 (t, J = 8.1 Hz, 1H), 7.05 (t, J = 2.2 Hz, 1H), 6.99 (dd, J = 8.3, 1.2 Hz, 1H), 6.88 (dd, J = 8.3, 2.5 Hz, 1H), 6.03 (s, 2H), 5.36(s, 2H). No desired ionization was observed in ESI or APCI modes.

4.2.18. 3-((4-Chlorophenoxy)methyl)-1-trityl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (46g)

Compound 46g was prepared from 45 as described for compound 46a. ¹H NMR (600 MHz, CDCl₃) δ 8.05 (s, 1H), 7.28–7.21 (m, 17H), 6.92 (dd, J = 8.9, 2.4 Hz, 2H), 6.26 (s, 2H), 5.33 (s, 2H). No desired ionization was observed in ESI or APCI modes.

4.2.19. 3-(Phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (47a)

Et₃SiH (4.4 mL, 28 mmol) and then TFA (5.3 mL, 69 mmol) were added dropwise to a solution of 46a (3.35 g, 6.93 mmol) in anhydrous CH₂Cl₂ (140 mL) at 0 °C. The resulting mixture was stirred at 0 °C for 30 min and then at room temperature for 2 h. After concentration, the residue was co-evaporated with toluene (100 mL × 2), and the resulting solid was triturated with warm hexanes (100 mL) and saturated NaHCO₃ (20 mL). The mixture was filtered and the solid was washed with hexanes (25 mL × 2) and water (10 mL × 2), suction-dried, and dried in vacuo to give compound 47a as a pale solid (1.61 g, 96%). ¹H NMR (600 MHz, DMSO-d₆) δ 13.56 (s, 1H), 8.21 (s, 1H), 7.35–7.27 (m, 2H), 7.07– 7.05 (m, 2H), 6.96 (t, J = 7.3 Hz, 1H), 5.43 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₂H₁₂N₅O [M + H]⁺ 242.1036, found 242.1046.

4.2.20. 3-((o-Tolyloxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (47b)

Compound 47b was prepared from 46b (421 mg, 0.846 mmol) as described for compound 47a. Pale solid, 190 mg, yield 88%. ¹H NMR (600 MHz, DMSO-d₆) δ 13.40 (s, 1H), 8.17 (s, 1H), 7.15–7.10 (m, 3H), 6.85 (t, J = 7.4 Hz, 1H), 5.42 (s, 2H), 2.15 (s, 3H). HRMS (ESI⁺) m/z calcd for C₁₃H₁₄N₅O [M + H]⁺ 256.1193, found 256.1205.

4.2.21. 3-((m-Tolyloxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (47c)

Compound 47c was prepared from 46c (371 mg, 0.746 mmol) as described for compound 47a. Pale solid, 179 mg, yield 94%. ¹H NMR (600 MHz, DMSO-d₆) δ 13.66 (s, 1H), 8.25 (s, 1H), 7.17 (t, J = 7.9 Hz, 1H), 6.89–6.78 (m, 3H), 5.41 (s, 2H), 2.27 (s, 3H). HRMS (ESI⁺) m/z calcd for C₁₃H₁₄N₅O [M + H]⁺ 256.1193, found 256.1192.

4.2.22. 3-((p-tolyloxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (47d)

Compound 47d was prepared from 46d (417 mg, 0.838 mmol) as described for compound 47a. White solid, 196 mg, yield 92%. ¹H NMR (600 MHz, DMSO-d₆) δ 13.65 (s, 1H), 8.24 (s, 1H), 7.09 (d, J = 8.1 Hz, 2H), 6.94 (d, J = 8.1 Hz, 2H), 5.40 (s, 2H), 2.22 (s, 3H). HRMS (ESI⁺) m/z calcd for C₁₃H₁₄N₅O [M + H]⁺ 256.1193, found 256.1201.

4.2.23. 3-((2-Chlorophenoxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (47e)

Compound 47e was prepared from 46e as described for compound 47a. ¹H NMR (600 MHz, CDCl₃) δ 10.80 (s, 1H), 8.34 (s, 1H), 7.41 (dd, J = 8.0, 1.2 Hz, 1H), 7.22 (td, J = 8.0, 1.2 Hz, 1H), 7.11 (d, J = 8.0 Hz, 1H), 6.99 (t, J = 7.8 Hz, 1H), 5.52 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₂H₁₁ClN₅O [M + H]⁺ 276.0647, found 276.0637.

4.2.24. 3-((3-Chlorophenoxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (47f)

Compound 47f was prepared from 46f as described for compound 47a. ¹H NMR (600 MHz, CDCl₃) δ 10.54 (s, 1H), 8.39 (s, 1H), 7.23 (t, J = 8.1 Hz, 1H), 7.06 (t, J = 2.1 Hz, 1H), 7.01 (ddd, J = 8.2, 2.1, 0.8 Hz, 1H), 6.94 (ddd, J = 8.1, 2.1, 0.8 Hz, 1H), 6.05 (s, 2H), 5.43 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₂H₁₁ClN₅O [M + H]⁺ 276.0647, found 276.0647.

4.2.25. 3-((4-Chlorophenoxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (47g)

Compound 47g was prepared from 46g as described for compound 47a. ¹H NMR (600 MHz, CDCl₃) δ 10.63 (s, 1H), 8.39 (s, 1H), 7.26 (d, J = 9.0 Hz, 2H), 6.98 (d, J = 9.0 Hz, 2H), 5.42 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₂H₁₁ClN₅O [M + H]⁺ 276.0647, found 276.0657.

4.2.26. 1-(4-Nitrobenzyl)-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (6)

Cs₂CO₃ (216 mg, 0.663 mmol) and 4-nitrobenzyl bromide (88 mg, 0.41 mmol) were added to a suspension of 47a (80 mg, 0.33 mmol) in anhydrous CH₃CN (4 mL). The resulting mixture was stirred at room temperature for 6 h and concentrated, then the residue was then dissolved in EtOAc (20 mL). The organic layer was washed with water (10 mL × 3) and brine (20 mL) and dried over Na₂SO₄. After filtration, the filtrate was concentrated, and the residue was purified by flash column chromatography (0–5% MeOH/CH₂Cl₂) to give compound 6 as a pale solid (70 mg, 56%). ¹H NMR (600 MHz, CDCl₃) δ 8.36 (s, 1H), 8.16 (d, J = 8.4 Hz, 2H), 7.41 (d, J = 8.4 Hz, 2H), 7.32– 7.29 (m, 2H), 7.05–7.01 (m, 3H), 6.27 (s, 2H), 5.64 (s, 2H), 5.40 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₉H₁₇N₆O₃ [M + H]⁺ 377.1357, found 377.1360.

4.2.27. 1-Benzyl-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (7)

Compound 7 was prepared from 47a (49 mg, 0.20 mmol) and benzyl bromide (32 µL, 0.27 mmol) as described for compound 6. White solid, 9 mg, yield 13%. ¹H NMR (600 MHz, CDCl₃) δ 8.37 (s, 1H), 7.31–7.28 (m, 7H), 7.03–7.01 (m, 3H), 6.22 (s, 2H), 5.55 (s, 2H), 5.40 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₉H₁₈N₅O [M + H]⁺ 332.1506, found 332.1504.

4.2.28. 1-(2-Nitrobenzyl)-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (8)

Compound 8 was prepared from 47a (100 mg, 0.414 mmol) and 2-nitrobenzyl bromide (107 mg, 0.495 mmol) as described for compound 6. White solid, 84 mg, yield 54%. ¹H NMR (600 MHz, CDCl₃) δ 8.35 (s, 1H), 8.17–8.16 (m, 1H), 7.46–7.43 (m, 2H), 7.33–7.30 (m, 2H), 7.05–7.02 (m, 3H), 6.62–6.60 (m, 1H), 6.15 (s, 2H), 6.03 (s, 2H), 5.43 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₉H₁₇N₆O₃ [M + H]⁺ 377.1357, found 377.1361.

4.2.29. 1-(3-Nitrobenzyl)-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (9)

Compound 9 was prepared from 47a (80 mg, 0.33 mmol) and 3-nitrobenzyl bromide (88 mg, 0.41 mmol) as described for compound 6. White solid, 63 mg, yield 50%. ¹H NMR (600 MHz, CDCl₃) δ 8.37 (s, 1H), 8.20 (t, J = 2.0 Hz, 1H), 8.15 (ddd, J = 8.2, 2.0, 1.1 Hz, 1H), 7.62 (ddd, J = 7.8, 1.8, 1.1 Hz, 1H), 7.49 (t, J = 7.9 Hz, 1H), 7.32–7.29 (m, 2H), 7.04–7.01 (m, 3H), 6.21 (s, 2H), 5.64 (s, 2H), 5.41 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₉H₁₇N₆O₃ [M + H]⁺ 377.1357, found 377.1357.

4.2.30. 1-(2-Aminobenzyl)-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (10)

SnCl₂ (198 mg, 1.04 mmol) was added to a suspension of 8 (56 mg, 0.15 mmol) in EtOH (5 mL). The resulting mixture was heated at 70 °C for 18 h, allowed to cool to room temperature, and diluted with EtOAc (12 mL). The reaction was carefully quenched with a NaHCO₃ solution (6 mL of saturated NaHCO₃ and 1.5 mL of water). The mixture was filtered through a pad of Celite and washed with 5% MeOH/EtOAc. The filtrate was separated, and the organic layer was washed with brine (20 mL × 2) and dried over Na₂SO₄. After filtration, the filtrate was concentrated, and the residue was purified by flash column chromatography (0–10% MeOH/CH₂Cl₂) to give compound 10 as a pale solid (41 mg, 79%). ¹H NMR (600 MHz, DMSO-d₆) δ 8.24 (s, 1H), 7.84 (s, 2H), 7.31–7.28 (m, 2H), 7.06–7.04 (m, 2H), 6.99–6.95 (m, 2H), 6.79 (dd, J = 7.6, 1.6 Hz, 1H), 6.65 (dd, J = 8.0, 1.2 Hz, 1H), 6.47 (td, J = 7.6, 1.2 Hz, 1H), 5.42 (s, 2H), 5.31 (s, 2H), 5.29 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₉H₁₉N₆O [M + H]⁺ 347.1615, found 347.1615.

4.2.31. 1-(3-Aminobenzyl)-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (11)

Compound 11 was prepared from 9 (48 mg, 0.13 mmol) as described for compound 10. White solid, 34 mg, yield 77%. ¹H NMR (600 MHz, DMSO-d₆) δ 8.23 (s, 1H), 7.75 (s, 2H), 7.31–7.28 (m, 2H), 7.06–7.04 (m, 2H), 6.96 (td, J = 7.3, 1.1 Hz, 1H), 6.92 (t, J = 7.7 Hz, 1H), 6.43 (ddd, J = 8.0, 2.2, 1.2 Hz, 1H), 6.40 (s, 1H), 6.36 (dd, J = 7.7, 1.2 Hz, 1H), 5.41 (s, 2H), 5.31 (s, 2H), 5.06 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₉H₁₉N₆O [M + H]⁺ 347.1615, found 347.1620.

4.2.32. 1-(4-Aminobenzyl)-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-pmine (12)

Compound 12 was prepared from 6 (58 mg, 0.15 mmol) as described for compound 10. Pale solid, 37 mg, yield 69%. ¹H NMR (600 MHz, DMSO-d₆) δ 8.22 (s, 1H), 7.83 (s, 2H), 7.30–7.27 (m, 2H), 7.04 (d, J = 8.4 Hz, 2H), 6.97–6.94 (m, 3H), 6.46 (d, J = 8.4 Hz, 2H), 5.40 (s, 2H), 5.27 (s, 2H), 5.04 (2H). HRMS (ESI⁺) m/z calcd for C₁₉H₁₉N₆O [M + H]⁺ 347.1615, found 347.1616.

4.2.33. 3-(Phenoxymethyl)-1-(4-(trifluoromethyl)benzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (13)

Compound 13 was prepared from 47a (40 mg, 0.17 mmol) and 4-(trifluoromethyl)benzyl bromide (50 mg, 0.21 mmol) as described for compound 6. White solid, 32 mg, yield 48%. ¹H NMR (600 MHz, CDCl₃) δ 8.37 (s, 1H), 7.56 (d, J = 8.0 Hz, 2H), 7.39 (d, J = 8.0 Hz, 2H), 7.31–7.28 (m, 2H), 7.04–7.01 (m, 3H), 6.22 (s, 2H), 5.60 (s, 2H), 5.40 (s, 2H). HRMS (ESI⁺) m/z calcd for C₂₀H₁₇F₃N₅O [M + H]⁺ 400.1380, found 400.1375.

4.2.34. 1-(4-(Methylsulfonyl)Benzyl)-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (14)

Compound 14 was prepared from 47a (40 mg, 0.17 mmol) and 4-(methylsulfonyl)benzyl bromide (52 mg, 0.21 mmol) as described for compound 6. White solid, 23 mg, yield 34%. ¹H NMR (600 MHz, CDCl₃) δ 8.36 (s, 1H), 7.88 (d, J = 8.4 Hz, 2H), 7.46 (d, J = 8.4 Hz, 2H), 7.32–7.29 (m, 2H), 7.04–7.01 (m, 3H), 6.25 (s, 2H), 5.63 (s, 2H), 5.40 (s, 2H), 3.01 (s, 3H). HRMS (ESI⁺) m/z calcd for C₂₀H₂₀N₅O₃S [M + H]⁺ 410.1281, found 410.1289.

4.2.35. 4-((4-Amino-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)benzonitrile (15)

Compound 15 was prepared from 47a (40 mg, 0.17 mmol) and 4-cyanobenzyl bromide (39 mg, 0.20 mmol) as described for compound 6. White solid, 34 mg, yield 57%. ¹H NMR (600 MHz, CDCl₃) δ 8.35 (s, 1H), 7.60 (d, J = 8.2 Hz, 2H), 7.36 (d, J = 8.2 Hz, 2H), 7.31–7.29 (m, 2H), 7.04–7.01 (m, 3H), 6.26 (s, 2H), 5.59 (s, 2H), 5.39 (s, 2H). HRMS (ESI⁺) m/z calcd for C₂₀H₁₇N₆O [M + H]⁺ 357.1458, found 357.1467.

4.2.36. Methyl 2-((4-Amino-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)benzoate (16)

Compound 16 was prepared from 47a (100 mg, 0.41 mmol) and methyl 2-(bromomethyl)benzoate (115 mg, 0.50 mmol) as described for compound 6. White solid, 41 mg, yield 25%. ¹H NMR (600 MHz, CDCl₃) δ 8.34 (s, 1H), 8.03 (dd, J = 7.2, 2.0 Hz, 1H), 7.35–7.29 (m, 4H), 7.05–7.01 (m, 3H), 6.53 (dd, J = 7.3, 1.7 Hz, 1H), 6.25 (s, 2H), 6.05 (s, 2H), 5.44 (s, 2H), 3.94 (s, 3H). HRMS (ESI⁺) m/z calcd for C₂₁H₂₀N₅O₃ [M + H]⁺ 390.1561, found 390.1567.

4.2.37. Methyl 3-((4-Amino-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)benzoate (17)

Compound 17 was prepared from 47a (100 mg, 0.41 mmol) and methyl 3-(bromomethyl)benzoate (114 mg, 0.50 mmol) as described for compound 6. White solid, 75 mg, yield 46%. ¹H NMR (600 MHz, CDCl₃) δ 8.37 (s, 1H), 8.03 (d, J = 1.9 Hz, 1H), 7.95 (dd, J = 7.7, 1.5 Hz, 1H), 7.46 (dd, J = 7.7, 1.6 Hz, 1H), 7.38 (t, J = 7.7 Hz, 1H), 7.31–7.27 (m, 2H), 7.03–7.01 (m, 3H), 6.22 (s, 2H), 5.59 (s, 2H), 5.39 (s, 2H), 3.89 (s, 3H). HRMS (ESI⁺) m/z calcd for C₂₁H₂₀N₅O₃ [M + H]⁺ 390.1561, found 390.1562.

4.2.38. Methyl 4-((4-amino-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)benzoate (18)

Compound 18 was prepared from 47a (100 mg, 0.41 mmol) and methyl 4-(bromomethyl)benzoate (115 mg, 0.50 mmol) as described for compound 6. White solid, 80 mg, yield 50%. ¹H NMR (600 MHz, CDCl₃) δ 8.36 (s, 1H), 7.97 (d, J = 8.3 Hz, 2H), 7.32–7.28 (m, 4H), 7.03–7.01 (m, 3H), 6.23 (s, 2H), 5.60 (s, 2H), 5.40 (s, 2H), 3.89 (s, 3H). HRMS (ESI⁺) m/z calcd for C₂₁H₂₀N₅O₃ [M + H]⁺ 390.1561, found 390.1566.

4.2.39. 4-((4-Amino-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)benzamide (19)

A mixture of 18 (50 mg, 0.13 mmol), CaCl₂ (55 mg, 0.50 mmol), and 7 N NH₃/MeOH (8 mL) was heated at 90 °C for 24 h in a sealed tube and then allowed to cool to room temperature. The mixture was concentrated, and the residue was treated with 10% MeOH/CH₂Cl₂ (20 mL). The organic phase was concentrated, and the residue was purified by flash column chromatography (0–10% MeOH/CH₂Cl₂) to give compound 19 as a white solid (37 mg, 77%). ¹H NMR (600 MHz, DMSO-d₆) δ 8.23 (s, 1H), 7.92 (s, 1H), 7.79 (d, J = 8.4 Hz, 2H), 7.34 (s, 1H), 7.32–7.28 (m, 2H), 7.24 (d, J = 8.4 Hz, 2H), 7.04 (d, J = 8.4 Hz, 2H), 6.96 (t, J = 7.5 Hz, 1H), 5.55 (s, 2H), 5.43 (s, 2H). HRMS (ESI⁺) m/z calcd for C₂₀H₁₉N₆O₂ [M + H]⁺ 375.1564, found 375.1558.

4.2.40. 1-((2-Chloropyridin-4-yl)methyl)-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (20)

Compound 20 was prepared from 47a (80 mg, 0.33 mmol) and 4-(bromomethyl)-2-chloropyridine [21] (85 mg, 0.41 mmol) as described for compound 6. Pale solid, 52 mg, yield 43%. ¹H NMR (600 MHz, CDCl₃) δ 8.36 (s, 1H), 8.32 (dd, J = 5.1, 0.7 Hz, 1H), 7.33–7.30 (m, 2H), 7.16 (d, J = 0.8 Hz, 1H), 7.06 (dd, J = 5.1, 0.7 Hz, 1H), 7.04–7.01 (m, 3H), 6.24 (s, 2H), 5.53 (s, 2H), 5.41 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₈H₁₆ClN₆O [M + H]⁺ 367.1069, found 367.1078.

4.2.41. 1-((6-Chloropyridin-3-yl)methyl)-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (21)

Compound 21 was prepared from 47a (80 mg, 0.33 mmol) and 5-(bromomethyl)-2-chloropyridine [21] (85 mg, 0.41 mmol) as described for compound 6. White solid, 47 mg, yield 38%. ¹H NMR (600 MHz, CDCl₃) δ 8.45 (d, J = 2.5 Hz, 1H), 8.36 (s, 1H), 7.61 (dd, J = 8.3, 2.5 Hz, 1H), 7.31–7.29 (m, 2H), 7.26 (d, J = 8.3 Hz, 1H), 7.04–7.01 (m, 3H), 6.20 (s, 2H), 5.52 (s, 2H), 5.37 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₈H₁₆ClN₆O [M + H]⁺ 367.1069, found 367.1070.

4.2.42. 1-((2-Aminopyridin-4-yl)methyl)-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (22)

TFA (2 mL) was added dropwise to a solution of 24 (29 mg, 0.065 mmol) in anhydrous CH₂Cl₂ (4 mL) at room temperature. The resulting mixture was stirred at room temperature for 1 h and then concentrated. The residue was treated with strong ammonia (1 mL) and then purified by flash column chromatography (0–15% MeOH/CH₂Cl₂) to give compound 22 as a white solid (22 mg, 98%). ¹H NMR (600 MHz, DMSO-d₆) δ 8.25 (s, 1H), 7.87 (d, J = 6.4 Hz, 1H), 7.68 (s, 2H), 7.33–7.30 (m, 2H), 7.07–7.05 (m, 2H), 6.98 (t, J = 7.2 Hz, 1H), 6.57 (d, J = 6.4 Hz, 1H), 6.45 (s, 1H), 5.53 (s, 2H), 5.44 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₈H₁₈N₇O [M + H]⁺ 348.1567, found 348.1563.

4.2.43. 1-((6-Aminopyridin-3-yl)methyl)-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (23)

Compound 23 was prepared from 25 (53 mg, 0.12 mmol) as described for compound 22. White solid, 30 mg, yield 73%. ¹H NMR (600 MHz, DMSO-d₆) δ 8.23 (s, 1H), 7.91 (s, 1H), 7.29–7.27 (m, 4H), 7.04–7.03 (m, 2H), 6.95 (t, J = 7.4 Hz, 1H), 6.36 (d, J = 8.5 Hz, 1H), 5.94 (s, 1H), 5.40 (s, 2H), 5.28 (s, 2H). HRMS (ESI⁺) m/z calcd for C₁₈H₁₈N₇O [M + H]⁺ 348.1567, found 348.1572.

4.2.44. Tert-Butyl (4-((4-Amino-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)pyridin-2-yl)carbamate (24)

Compound 24 was prepared from 47a (100 mg, 0.41 mmol) and tert-butyl (4-(bromomethyl)pyridin-2-yl)carbamate [22] (143 mg, 0.50 mmol) as described for compound 6 except that DMF was used a reaction solvent. White solid, 42 mg, yield 23%. ¹H NMR (600 MHz, CDCl₃) δ 8.36 (s, 1H), 8.12 (d, J = 6.5 Hz, 1H), 8.00 (s, 1H), 7.93 (s,1H), 7.32–7.27 (m, 2H), 7.04–7.02 (m, 3H), 6.59 (s, 1H), 6.30 (s, 2H), 5.54 (s, 2H), 5.41 (s, 2H), 1.52 (s, 9H). HRMS (ESI⁺) m/z calcd for C₂₃H₂₆N₇O₃ [M + H]⁺ 448.2092, found 448.2097.

4.2.45. Tert-Butyl (5-((4-Amino-3-(phenoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)pyridin-2-yl)carbamate (25)

Compound 25 was prepared from 47a (100 mg, 0.41 mmol) and tert-butyl (5-(bromomethyl)pyridin-2-yl)carbamate [22] (143 mg, 0.50 mmol) as described for compound 6. White solid, 72 mg, yield 39%. ¹H NMR (600 MHz, CDCl₃) δ 8.37 (s, 1H), 8.30 (d, J = 2.4 Hz, 1H), 7.97 (s, 1H), 7.89 (d, J = 8.7 Hz, 1H), 7.67 (dd, J = 8.7, 2.4 Hz, 1H), 7.31–7.28 (m, 2H), 7.02–7.00 (m, 3H), 6.27 (s, 2H), 5.47 (s, 2H), 5.37 (s, 2H), 1.51 (s, 9H). HRMS (ESI⁺) m/z calcd for C₂₃H₂₆N₇O₃ [M + H]⁺ 448.2092, found 448.2096.

4.2.46. 1-(4-Nitrobenzyl)-3-((o-tolyloxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (26)

Compound 26 was prepared from 47b (45 mg, 0.176 mmol) and 4-nitrobenzyl bromide (46 mg, 0.21 mmol) as described for compound 6. Pale solid, 47 mg, yield 68%. ¹H NMR (600 MHz, CDCl₃) δ 8.37 (s, 1H), 8.17 (d, J = 8.7 Hz, 2H), 7.44 (d, J = 8.7 Hz, 2H), 7.18 (dd, J = 7.5, 1.7 Hz, 1H), 7.14 (td, J = 7.5, 1.7 Hz, 1H), 6.99 (d, J = 8.1 Hz, 1H), 6.94 (td, J = 7.5, 0.9 Hz, 1H), 6.22 (s, 2H), 5.65 (s, 2H), 5.39 (s, 2H), 2.28 (s, 3H). HRMS (ESI⁺) m/z calcd for C₂₀H₁₉N₆O₃ [M + H]⁺ 391.1513, found 391.1519.

4.2.47. 1-(4-Nitrobenzyl)-3-((m-tolyloxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (27)

Compound 27 was prepared from 47c (45 mg, 0.176 mmol) and 4-nitrobenzyl bromide (46 mg, 0.21 mmol) as described for compound 6. White solid, 36 mg, yield 52%. ¹H NMR (600 MHz, CDCl₃) δ 8.36 (s, 1H), 8.16 (d, J = 8.7 Hz, 2H), 7.42 (d, J = 8.7 Hz, 2H), 7.17 (td, J = 7.6, 0.9 Hz, 1H), 6.85–6.81 (m, 3H), 6.27 (s, 2H), 5.64 (s, 2H), 5.38 (s, 2H), 2.31 (s, 3H). HRMS (ESI⁺) m/z calcd for C₂₀H₁₉N₆O₃ [M + H]⁺ 391.1513, found 391.1519.

4.2.48. 1-(4-Nitrobenzyl)-3-((p-tolyloxy)methyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (28)

Compound 28 was prepared from 47d (45 mg, 0.176 mmol) and 4-nitrobenzyl bromide (46 mg, 0.21 mmol) as described for compound 6. White solid, 43 mg, yield 62%. ¹H NMR (600 MHz, CDCl₃) δ 8.36 (s, 1H), 8.16 (d, J = 8.7 Hz, 2H), 7.41 (d, J = 8.7 Hz, 2H), 7.09 (d, J = 8.6 Hz, 2H), 6.91 (d, J = 8.6 Hz, 2H), 6.28 (s, 2H), 5.63 (s, 2H), 5.26 (s, 2H), 2.29 (s, 3H). HRMS (ESI⁺) m/z calcd for C₂₀H₁₉N₆O₃ [M + H]⁺ 391.1513, found 391.1522.

4.2.49. 3-((2-Chlorophenoxy)methyl)-1-(4-nitrobenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (29)

Compound 29 was prepared from 47e (84 mg, 0.30 mmol) and 4-nitrobenzyl bromide (100 mg, 0.46 mmol) as described for compound 6. Pale solid, 103 mg, yield 84%. ¹H NMR (400 MHz, CDCl₃) δ 8.37 (s, 1H), 8.17 (d, J = 8.6 Hz, 2H), 7.43 (d, J = 8.6 Hz, 2H), 7.39 (dd, J = 8.0, 1.6 Hz, 1H), 7.18 (td, J = 8.0, 1.6 Hz, 1H), 7.08 (dd, J = 8.0, 1.6 Hz, 1H), 6.97 (td, J = 7.7, 1.5 Hz, 1H), 6.24 (s, 2H), 5.64 (s, 2H), 5.48 (s, 2H). ¹³C NMR (100 MHz, CDCl₃) δ 158.2, 157.1, 155.5, 152.7, 147.8, 143.7, 141.4, 130.8, 128.8, 128.2, 124.1, 123.1, 122.7, 114.1, 99.9, 65.7, 49.9. HRMS (ESI⁻) m/z calcd for C₁₉H₁₄ClN₆O₃ [M-H]⁻ 409.0821, found 409.0837.

4.2.50. 3-((3-Chlorophenoxy)methyl)-1-(4-nitrobenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (30)

Compound 30 was prepared from 47f (45 mg, 0.16 mmol) and 4-nitrobenzyl bromide (53 mg, 0.24 mmol) as described for compound 6. Pale solid, 41 mg, yield 63%. ¹H NMR (400 MHz, CDCl₃) δ 8.37 (s, 1H), 8.17 (d, J = 8.7 Hz, 2H), 7.43 (d, J = 8.7 Hz, 2H), 7.21 (t, J = 8.1 Hz, 1H), 7.25–6.97 (m, 2H), 6.90 (dd, J = 8.3, 0.9 Hz, 1H), 6.14 (s, 2H), 5.64 (s, 2H), 5.40 (s, 2H). ¹³C NMR (100 MHz, CDCl₃) δ 158.0, 157.9, 157.0, 155.4, 147.8, 143.6, 141.5, 135.5, 130.8, 128.7, 124.2, 122.8, 115.6, 113.5, 99.8, 65.3, 49.9. HRMS (ESI⁻) m/z calcd for C₁₉H₁₄ClN₆O₃ [M-H]⁻ 409.0821, found 409.0839.

4.2.51. 3-((4-Chlorophenoxy)methyl)-1-(4-nitrobenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine (31)

Compound 31 was prepared from 47g (47 mg, 0.17 mmol) and 4-nitrobenzyl bromide (60 mg, 0.28 mmol) as described for compound 6. Pale solid, 39 mg, yield 57%. ¹H NMR (400 MHz, DMSO-d₆) δ 8.23 (s, 1H), 8.17 (d, J = 8.8 Hz, 2H), 7.41 (d, J = 8.8 Hz, 2H), 7.33 (d, J = 9.0 Hz, 2H), 7.06 (d, J = 9.0 Hz, 2H), 5.65 (s, 2H), 5.43 (s, 2H). ¹³C NMR (100 MHz, DMSO-d₆) δ 157.9, 156.5, 156.4, 154.7, 146.9, 144.6, 140.8, 129.2, 128.5, 125.0, 123.7, 116.9, 98.5, 63.8, 49.0. HRMS (ESI⁻) m/z calcd for C₁₉H₁₄ClN₆O₃ [M-H]⁻ 409.0821, found 409.0831.

4.3. Antiviral Assays

The ZIKV reporter assay and titer-reduction assay were performed as previously reported [17]. Briefly, Huh7 cells (1.5 × 10⁴) were seeded in a 96-well plate and inoculated with a luciferase reporter ZIKV (MOI=0.2) [17]. After two hours, the cells were treated with medium containing the compound (10 µM). After 3 days post-infection, the cells were lysed, the Nanoluc signal was detected using the Nano-Glo^® luciferase assay (Promega), then measured using a Neo 2 plate reader (BioTek, Winooski, VT, USA). For titer-reduction assays, 1.5 × 10⁵ Huh7 cell were seeded in a 24-well plate. Next day, the cells were inoculated with ZIKV for two hours. The inoculum was replaced with compound-containing medium (8.5 µM) and incubated for 3 days. Supernatants were collected and viral titers were estimated by plaque assay.

4.4. Cell Viability (CC₅₀) Assay

The cell viability assay was performed in Huh7 cells as previously reported [17]. Briefly, non-infected Huh7 cells were treated with the testing compounds for 3 days. Viability was measured by absorbance at 490 mM using the MTS-based tetrazolium reduction CellTiter 96 Aqueous Non-Radioactive cell proliferation assay (Promega).