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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250643Generated: October 26, 2026

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

https://huagongshe.com/reaction/1250643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Butylamino-2-chloro-7-methylthieno[3,2-d]pyrimidineHCID 18326389—
Product2-Allylamino-4-butylamino-7-methylthieno[3,2-d]pyrimidineHCID 1832639573.9%

Reaction Steps

In a sealed tube were heated 307 mg (1.2 mmol) of 4-butylamino-2-chloro-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=1/8) to give 245 mg (yield: 73.8%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-4764e4e0f5c947428a00b3e0d2c556f7
Source noteuspto-grants-2002_01