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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250693Generated: October 30, 2026

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

https://huagongshe.com/reaction/1250693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Chloro-4-dodecylamino-7-methylthieno[3,2-d]pyrimidineHCID 18326380—
Product2-Allylamino-4-dodecylamino-7-methylthieno[3,2-d]pyrimidineHCID 1832655544.8%

Reaction Steps

442 mg (1.2 mmol) of 2-chloro-4-dodecylamino-7-methylthieno[3,2-d]pyrimidine and 1.10 g (19.2 mmol) of allylamine were heated in a sealed tube at 140° 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 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 209 mg (yield: 44.8%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-b78d7a3e5a164c2ea92562478c212581
Source noteuspto-grants-2002_01