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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262310Generated: November 3, 2026

Acetic Acid → 2-Bromo-1-(2-chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)ethanone

https://huagongshe.com/reaction/2262310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen BromideHCID 260—
ReactantBromineHCID 24408—
Reactant1-(2-Chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)ethanoneHCID 59593157—
SolventChloroformHCID 6212—
Product2-Bromo-1-(2-chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)ethanoneHCID 59592905—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-(2-chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)ethanone (1.0 eq) dissolved in a mixture of CHCl3, 33% wt HBr and acetic acid (1:1:1) at −0° C. was added a solution of Br2 in CHCl3 (1.05 eq). Reaction mixture was stirred at −0° C. until completed, then extracted in dichloromethane with saturated bicarbonate solution one time. The organic layer is dried, filtered and concentrated to yield the crude intermediate. This intermediate is purified by flash chromatography to yield 2-bromo-1-(2-chloro-4-morpholinothieno[3,2-d]pyrimidin-6-yl)ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846929B2
Source datasetuspto-grants-2010_12
ORD IDord-4b4ab6877694436d871d5d07ceb8ab73
Source noteuspto-grants-2010_12