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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681629Generated: October 26, 2026

Dimethylformamide → 3,7-Dihydro-6-methylthio-3-n-propyl-2H-purin-2-one

https://huagongshe.com/reaction/1681629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant3-Propyl-6-thioxanthineHCID 14014540—
SolventEthanolHCID 702—
SolventHexaneHCID 8058—
Product3,7-Dihydro-6-methylthio-3-n-propyl-2H-purin-2-oneHCID 10443612—

Reaction Steps

In an argon atmosphere(9.77 g (244 mmol) of 60% sodium hydride was washed with n-hexane 3 times. The solvent was evaporated under reduced pressure and dried. After 900 ml of N,N'-dimethylformamide was added 57.0 g (271 mmol) of 3-n-propyl-6-thioxanthine (Japanese Published Unexamined Patent Application No. 183287/86) was gently added under ice cooling. 15 minutes after, 15.2 ml (244 mmol) of methyl iodide was dropwise added to the reaction mixture. After stirring for 30 minutes, 50 ml of ethanol was added and the mixture was concentrated under reduced pressure. Then 400 ml of water was added and precipitates were collected by filtration to give 13.9 g (yield, 23%) of Compound b as light yellow powder. The filtrate was extracted 5 times with 200 ml of chloroform. After washing with a saturated aqueous sodium chloride solution, the extract was dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: 10% methanol/chloroform) to give further 16.0 g (yield, 26%) of Compound b as a light yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05173492
Source datasetuspto-grants-1992_12
ORD IDord-18cf1bffabd743579d1217e015e5bfba
Source noteuspto-grants-1992_12