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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864996Generated: November 1, 2026

Water → (-)-2-(2-Amino-6-chloropurin-9-ylmethyl)-1,4-butanediol

https://huagongshe.com/reaction/864996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium borohydrideHCID 4148881—
ReactantDimethyl 2-(2-amino-6-chloropurin-9-ylmethyl)succinateHCID 19027590—
Solventtert-ButanolHCID 6386—
Product(-)-2-(2-Amino-6-chloropurin-9-ylmethyl)-1,4-butanediolHCID 19027588100%

Reaction Steps

To a solution of (-)-dimethyl-2-(2-amino-6-chloropurin-9-ylmethyl)succinate (enantiomeric excess 85%; 19.9 mg, 0.0607 mmol), dissolved in tert. butanol (2.0 ml) at 40° C., was added lithium borohydride (30 mg, 1.38 mmol) in portions with stirring After 1 h at ambient temperature, water (0.3 ml) was added slowly and stirring continued over night. Inorganic salts were filtered, washed carefully with tert. butanol and the solution was evaporated to dryness. Preparative thin-layer chromatography (PSC-Fertigplatten, Merck) with chloroform+methanol (5+1) as mobile phase afforded 16.5 mg (theoretical yield) of (-)-2-(2-amino-6-chloropurin-9-ylmethyl)-1,4-butanediol. [α]D20 ° -5.20°, [α]54620 -5.92° (c 0.625, ethanol). TLC on silica (chloroform+methanol 5+1): Rf 0.40, identical to that of the racemate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565461
Source datasetuspto-grants-1996_10
ORD IDord-81a85e290ed74a21adbd898cea44a784
Source noteuspto-grants-1996_10