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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516282Generated: November 4, 2026

Methanol → HCID 44230606, compound

https://huagongshe.com/reaction/1516282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 57867403HCID 57867403—
SolventAmmoniaHCID 222—
ProductHCID 44230606HCID 4423060686%

Reaction Steps

A solution of ((2R,4R)-3-acetoxy-5-(6-(cyclohexylamino)-9H-purin-9-yl)-4-fluoro-3,4-dimethyltetrahydrofuran-2-yl)methyl benzoate (about 0.32 g, 0.60 mmol) in methanolic ammonia (25% w/w 15 ml) was stirred at room temperature for overnight. Completion of the reaction monitored by thin-layer chromatography and methanol was removed under reduced pressure then water added to the crude and extracted with ethyl acetate. The organic layer was dried over sodium sulphate, concentrated under reduced pressure and purified by silica gel column chromatography using 5% Methanol in dichloromethane to elude title compound (0.2 g) as a colorless solid. Yield: 86%; 1H NMR (300 MHz, CDCl3): δ 8.32 (s, 1H), 7.93 (d, 1H, J=3.3 Hz), 6.60 (d, 1H, J=22.5 Hz), 5.79 (bs, 1H), 5.51 (s, 1H), 5.23 (bs, 1H), 4.25-4.13 (m, 3H), 2.17-2.04 (m, 1H), 1.76-1.52 (m, 16H); ES Mass: [M+1]+ 380 (100%), 381 (45%); IR cm−: 3338, 2928, 2854, 1624, 1475, 1226, 1062, 938, 740; HPLC: 97.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227431B2
Source datasetuspto-grants-2012_07
ORD IDord-28fd3620205f481d81d38635c196e409
Source noteuspto-grants-2012_07