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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250690Generated: October 31, 2026

Allylamine → 2,4-Diallylamino-7-bromothieno[3,2-d]pyrimidine

https://huagongshe.com/reaction/1250690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Allylamino-7-bromo-2-chlorothieno[3,2-d]pyrimidineHCID 18326469—
Product2,4-Diallylamino-7-bromothieno[3,2-d]pyrimidineHCID 1832642093.5%

Reaction Steps

305 mg (1.0 mmol) of 4-allylamino-7-bromo-2-chlorothieno[3,2-d]pyrimidine and 914 mg (16.0 mmol) of allylamine were heated in a sealed tube at 160° C. for 16 hours. After completion of the reaction, the reaction mixture was allowed to resume room temperature, followed by adding a saturated aqueous sodium hydrogen carbonate solution thereto and extraction with ethyl acetate (50 ml×2). After the organic layer was washed with brine and dried over anhydrous sodium sulfate, the solvent was distilled off. The residue was purified by silica gel chromatography (eluent: ethyl acetate-hexane=1/4) to give 304 mg (yield: 93.3%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-8620769b61f349f98f2a768d30fe6ecb
Source noteuspto-grants-2002_01