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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408986Generated: November 1, 2026

Phosphorus oxychloride → 7-Chloro-2-(Methylsulfanyl)-[1,3]thiazolo[4,5-d]pyriMidine

https://huagongshe.com/reaction/2408986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-(methylthio)thiazolo[4,5-d]pyrimidin-7(6h)-oneHCID 135500690—
Product7-Chloro-2-(Methylsulfanyl)-[1,3]thiazolo[4,5-d]pyriMidineHCID 1435938886%

Reaction Steps

A mixture of 2-(methylthio)thiazolo[4,5-d]pyrimdin-7-(6H)-one (800 mg) and phosphorous oxychloride (8 mL) was refluxed for 2 h. Solvents were removed under vacuum and the mixture was diluted with chloroform. Again the solvents were removed under vacuum and this procedure repeated twice (yellow color solid). The residue was diluted with ice cold water and basified with 10% aqueous sodium bicarbonate. The solution was extracted with chloroform (3×100 mL) and the combined chloroform layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using hexane-ethyl acetate (95:5) as eluents to give the product as a white color solid (750 mg, 86%), mp 148-150° C. 1H NMR (400 MHz, CDCl3): δ 8.95 (1H, s), 2.90 (3H, s); LC-MS (positive ion mode): m/z 218, 220 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815879B2
Source datasetuspto-grants-2014_08
ORD IDord-2956da1b6928415fb55bcaedad250e38
Source noteuspto-grants-2014_08