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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250634Generated: October 25, 2026

Allylamine → 2-Allylamino-4-ethylamino-7-methylthieno[3,2-d]pyrimidine

https://huagongshe.com/reaction/1250634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Chloro-4-ethylamino-7-methylthieno[3,2-d]pyrimidineHCID 18326403—
Product2-Allylamino-4-ethylamino-7-methylthieno[3,2-d]pyrimidineHCID 1832647764.3%

Reaction Steps

In a sealed tube were heated 273 mg (1.2 mmol) of 2-chloro-4-ethylamino-7-methylthieno[3,2-d]pyrimidine and 1.10 g (19.2 mmol) of allylamine at 160° C. for 16 hours. After completion of the reaction, the reaction mixture was allowed to resume room temperature, and a saturated aqueous sodium hydrogen carbonate solution was added thereto, followed by extraction with ethyl acetate (50 ml×2). The organic layer was washed with brine and dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent: ethyl acetate-hexane=1/2) to give 191 mg (yield: 64.3%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-f75b6658b69f41e5b67981c2462e5f32
Source noteuspto-grants-2002_01