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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250661Generated: November 2, 2026

Cyclohexylamine → HCID 18326406, compound

https://huagongshe.com/reaction/1250661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantHCID 18326385HCID 18326385—
SolventAcetonitrileHCID 6342—
ProductHCID 18326406HCID 1832640649.9%

Reaction Steps

122 mg (1.0 mmol) of N,N-dimethylaminopyridine was added to a solution of 306 mg (1.4 mmol) of di-t-butyldicarbonate in acetonitrile at room temperature, followed by stirring 20 minutes. After 220 mg (1.0 mmol) of 2-allylamino-4-amino-7-methylthieno[3,2-d]pyrimidine was added to the reaction solution, the mixture was stirred at room temperature for 2 hours. Further, 139 mg (1.4 mmol) of cyclohexylamine was added thereto, followed by heating under reflux for 16 hours. After completion of the reaction, the solvent was distilled off under reduced pressure. The residue was purified by a silica gel chromatography (eluent: ethyl acetate-hexane=1/4) to give 172 mg (yield: 49.9%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-d89d6565adf04903b5333dd30add7882
Source noteuspto-grants-2002_01