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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250639Generated: October 30, 2026

Amantadine → HCID 18326461, compound

https://huagongshe.com/reaction/1250639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmantadineHCID 2130—
Reactant2,4-Dichloro-7-methylthieno(3,2-d)pyrimidineHCID 7147064—
SolventDimethylformamideHCID 6228—
ProductHCID 18326461HCID 18326461103%

Reaction Conditions

Temperature0 °C

Reaction Steps

In DMF was dissolved 700 mg (3.2 mmol) of 2,4-dichloro-7-methylthieno[3,2-d]pyrimidine, and then an aqueous solution of 1.13 g (7.5 mmol) of 1-adamantaneamine was added dropwise to the resulting rid solution under ice cooling over 5 minutes. The reaction mixture was stirred at 0° C. for one hour and then allowed to resume room temperature, followed by stirring for one hour. After completion of the reaction, ice water was added to the reaction mixture, followed by extraction with ethyl acetate (50 ml×3). After the organic layer was washed successively with 1N hydrochloric acid, water and brine and dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent: ethyl acetate-hexane=1/10) to give 1.10 g (yield: 100%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-ae03ba3dda5941fb8cf2c47add1c9925
Source noteuspto-grants-2002_01