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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268435Generated: October 29, 2026

Methanol → 2-{9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}acetic acid

https://huagongshe.com/reaction/2268435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant2-{9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}acetonitrileHCID 59975293—
Product2-{9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}acetic acidHCID 59975282—

Reaction Steps

A stirred solution of 2-{9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}acetonitrile (preparation 30) (1.5 g, 3 mmol) in methanol (30 ml) and an aqueous 1 molar solution of sodium hydroxide (10 ml) was heated at reflux for 24 hr. The methanol was then removed under reduced pressure and the residual liquid diluted with more water and washed twice with ethyl acetate. The aqueous phase was acidified to pH<7 with a 1 molar aqueous citrc acid solution and then extracted twice with ethyl acetate. The extracts were combined, washed with brine and dried with anhydrous magnesium sulfate. The residue, after removal of the solvent under reduced pressure, was dissolved into diethyl ether and the solvent removed again twice under reduced pressure to give the title compound (1.25 g) as a foam. MS: 518 (M−H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326359B1
Source datasetuspto-grants-2001_12
ORD IDord-b9b1e6382cc04cbda5ebf4e8cd93ee2d
Source noteuspto-grants-2001_12