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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279210Generated: October 30, 2026

2-Naphthalenesulfonyl chloride → HCID 69557677, compound

https://huagongshe.com/reaction/1279210

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Naphthalenesulfonyl chlorideHCID 7125—
ReactantTriethylamineHCID 8471—
ReactantHCID 69558158HCID 69558158—
SolventDichloromethaneHCID 6344—
ProductHCID 69557677HCID 6955767749.7%

Reaction Steps

A solution of (3aS,4S,6R,6aR)-6-{2-(aminomethyl)-6-[(2,2-diphenylethyl)amino]-9H-purin-9-yl}-N-ethyl-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carboxamide (Preparation 10) (140 mg, 0.25 mmol) and triethylamine (0.05 ml, 0.36 mmol) in anhydrous dichloromethane (1 ml) was treated with a solution of 2-naphthalenesulfonyl chloride (63 mg, 0.28 mmol) in anhydrous dichloromethane (1 ml). The mixture was stirred at room temperature for 18 hours during which time the solvent was allowed to evaporate off freely. The residue was dissolved in ethanol (1 ml), treated with hydrochloric acid (1M, 1 ml) and heated at 60° C. for 15 hours. The solvent was removed under reduced pressure and the residue was azeotroped with ethanol (×2). The residue was then purified by column chromatography on silica gel eluting with a gradient system of dichloromethane:methanol (95:5 by volume) gradually changing to dichloromethane:methanol (90:10 by volume) to give a solid which was triturated with diethyl ether, diluted with pentane, filtered and dried to afford the title compound as a solid (88 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448236B1
Source datasetuspto-grants-2002_09
ORD IDord-21053c2fb46a4335831211573c3817d2
Source noteuspto-grants-2002_09