Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516270Generated: November 2, 2026

HCID 57867385, compound → HCID 57867369, compound

https://huagongshe.com/reaction/1516270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57867385HCID 57867385—
SolventWaterHCID 962—
ProductHCID 57867369HCID 5786736978.6%

Reaction Steps

A solution of ((2R,4R)-3-acetoxy-5-(6-(cycloheptylamino)-9H-purin-9-yl)-4-fluoro-3,4-dimethyltetrahydrofuran-2-yl)methyl benzoate (about 0.3 g, 0.55 mmol) in methanolicammonia (25% w/w 10 ml) was stirred at room temperature for overnight. Completion of the reaction mixture monitored by thin-layer chromatography, water added to the reaction mixture and the aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with brine and dried over sodium sulphate. Concentration under reduced pressure and purification by silica gel column chromatography using 25% ethyl acetate in hexane as eluent furnished title compound (0.17 g) as a colorless solid. Yield: 78%; 1H-NMR: 1H NMR (300 MHz, CDCl3): δ 8.34 (s, 1H), 7.95 (d, 1H, J=3.6 Hz), 6.59 (d, 1H, J=22.5 Hz), 5.80 (bs, 1H), 5.24 (s, 1H), 4.28-4.20 (m, 4H), 2.14-2.09 (m, 1H), 1.59-1.25 (m, 18H); ES Mass: [M+1]+ 394 (100%), 395 (30%); IR cm−: 3364, 2928, 2855, 2358, 1758, 1618, 1378, 1101, 844, 750; HPLC: 98.16%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227431B2
Source datasetuspto-grants-2012_07
ORD IDord-39c10d9fc7994266ab8a239661481271
Source noteuspto-grants-2012_07