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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19569Generated: October 26, 2026

Tetrahydrofuran → 4-Chloro-2-(methylsulfonyl)thieno[2,3-d]pyrimidine

https://huagongshe.com/reaction/19569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-Chloro-2-(methylthio)thieno[2,3-d]pyrimidineHCID 21988351—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-Chloro-2-(methylsulfonyl)thieno[2,3-d]pyrimidineHCID 21988354—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 1 L round-bottom flask was added 4-chloro-2-(methylthio)thieno[2,3-d]pyrimidine (35.0 g, 162 mmol), THF (300 mL). The solution was stirred at 0° C. and treated dropwise with a solution of OXONE (209 g, 339 mmol) in water (350 mL). The resulting mixture was stirred at RT overnight. The reaction mixture was diluted with EtOAc (500 mL) and water (300 mL). Separated the layers, the aqueous layer was extracted with EtOAc (3×300 mL). Organic layers were combined, washed with brine (2×300 mL), dried over MgSO4, filtered and concentrated to give (33 g). MS (ES+): 249 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745449B2
Source datasetuspto-grants-2010_06
ORD IDord-03422f858edf4ef7aae928893ffd282e
Source noteuspto-grants-2010_06