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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518792Generated: October 30, 2026

Potassium Carbonate → 7-(4-Fluorophenyl)-2-(methylsulfonyl)thieno[3,2-d]pyrimidine-6-carboxamide

https://huagongshe.com/reaction/518792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
Reactant7-(4-Fluorophenyl)-2-(methylsulfanyl)thieno[3,2-d]pyrimidine-6-carboxamideHCID 86697962—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product7-(4-Fluorophenyl)-2-(methylsulfonyl)thieno[3,2-d]pyrimidine-6-carboxamideHCID 8669796160.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 135 mg of 7-(4-fluorophenyl)-2-(methylsulfanyl)thieno[3,2-d]pyrimidine-6-carboxamide and 293 mg of sodium perborate tetrahydrate in 5 ml of acetic acid is microwave-heated at 70° C. in a sealed tube for 1 h 30. The mixture is taken up with dichloromethane and 100 ml of a sodium thiosulfate solution. The pH is adjusted to pH 8-9 by adding solid potassium carbonate and the aqueous phase is extracted with dichloromethane. The organic phases are dried over magnesium sulfate, filtered, and then concentrated under vacuum so as to obtain a beige solid. This crude is purified on 40 g of silica, elution being carried out with dichloromethane, so as to obtain 90 mg of 7-(4-fluorophenyl)-2-(methylsulfonyl)thieno[3,2-d]pyrimidine-6-carboxamide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115140B2
Source datasetuspto-grants-2015_08
ORD IDord-d90349b41c374309adeac0fc0b733c66
Source noteuspto-grants-2015_08