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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105766Generated: November 2, 2026

Acetonitrile → HCID 58999043, compound

https://huagongshe.com/reaction/2105766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantCyclohexane, (bromomethyl)-HCID 137636—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 68838889HCID 68838889—
ProductHCID 58999043HCID 58999043—

Reaction Steps

To a suspension of 90 mg of 2-(2-chloro-phenyl)-5-methyl-1H-imidazole-4-carboxylic acid piperidin-1-ylamide in 4 ml of acetonitrile was added 35 mg of potassium tert-butylate and the reaction mixture was stirred at room temperature for 2 minutes. After such time, 0.04 ml of (bromomethyl)cyclohexane was added and the reaction mixture was stirred at 80° C. for 28 hours under argon atmosphere. The reaction mixture was then concentrated in vacuo and purified by column chromatography (SiO2, Heptane/EtOAC:1/1) to give 64 mg of the title compound as a pale yellow solid, MS (ISP) 415.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579369B2
Source datasetuspto-grants-2009_08
ORD IDord-d52f60324a674bbe8b7d668c62d0b1ac
Source noteuspto-grants-2009_08