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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250623Generated: October 26, 2026

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

https://huagongshe.com/reaction/1250623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
Reactant4-Benzylamino-2-chloro-7-methylthieno[3,2-d]pyrimidineHCID 18326454—
SolventWaterHCID 962—
Product2-Allylamino-4-benzylamino-7-methylthieno[3,2-d]pyrimidineHCID 1832643481.3%

Reaction Conditions

Temperature140 °C

Reaction Steps

In 2.28 g (40.0 mmol) of allylamine was dissolved 250 mg (0.9 mmol) of 4-benzylamino-2-chloro-7-methylthieno[3,2-d]pyrimidine, and the resulting solution was heated in a sealed tube at 140° C. for 24 hours. After the reaction mixture was cooled, 100 ml of water was added thereto, followed by extraction with ethyl acetate (20 ml×3). The organic layer was washed with 20 ml of water and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The residue was purified by silica gel column chromatography (eluent: ethyl acetate-hexane=1/4) to give 217 mg (yield: 81.3%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-43f2b943b3114253b4617cd006c80fd1
Source noteuspto-grants-2002_01