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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018642Generated: October 26, 2026

Ammonia → 1-(3,5-Bis-trifluoromethyl-benzoyl)-4-(3-chloro-phenylamino)-piperidine-4-carbonitrile

https://huagongshe.com/reaction/1018642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant3-ChloroanilineHCID 7932—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant1-(3,5-Bis(trifluoromethyl)benzoyl)piperidin-4-oneHCID 11209963—
SolventAcetic AcidHCID 176—
Product1-(3,5-Bis-trifluoromethyl-benzoyl)-4-(3-chloro-phenylamino)-piperidine-4-carbonitrileHCID 1840163474.3%

Reaction Steps

To a solution of 1-(3,5-bis-trifluoromethyl-benzoyl)-piperidin-4-one (5.1 g, 15 mmol) in acetic acid (20 mL) were added with cooling 3-chloroaniline (1.7 mL, 16.5 mmol) and trimethylsilylcyanide (1.9 mL, 15 mmol) so that the temperature did not rise above 20° C. The suspension was stirred for 6 h at room temperature. The reaction mixture was than added to ice-water (350 mL), ammonia (55 mL, 25%) was added to the mixture which was stirred for 15 min. After that the mixture was extracted with dichloromethane, the organic phases were pooled, washed with brine and dried with MgSO4. The solvent was evaporated and the residue crystallized from ethylacetate to yield the desired product (5.3 g, 74%), m.p. 205-207° C. and MS: m/e=476.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482829B2
Source datasetuspto-grants-2002_11
ORD IDord-0cc7c83b72344655b74f70b1e01513f1
Source noteuspto-grants-2002_11