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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857659Generated: November 3, 2026

1,1'-Carbonyldiimidazole → N-[2-(3,4-Dichlorophenyl)-2-(4-hydroxy-4-phenyl-piperidino)ethyl]-N-methyl-3,5-bis(trifluoromethyl)phenylacetamide hydrochloride salt

https://huagongshe.com/reaction/1857659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3,5-Bis(trifluoromethyl)phenylacetic acidHCID 123587—
ReactantHCID 15434904HCID 15434904—
SolventTetrahydrofuranHCID 8028—
ProductN-[2-(3,4-Dichlorophenyl)-2-(4-hydroxy-4-phenyl-piperidino)ethyl]-N-methyl-3,5-bis(trifluoromethyl)phenylacetamide hydrochloride saltHCID 2212965848%

Reaction Conditions

Temperature23 °C

Reaction Steps

A solution of 3,5-bis(trifluoromethyl)phenylacetic acid (1.61 g) and 1,1'-carbonyldiimidazole (1.01 g) in tetrahydrofuran (15 mL) was stirred at reflux for 0.5 hours. The reaction was cooled to 23° C. and treated with a solution of N-[2-(3,4-dichlorophenyl)-2-(4-hydroxy-4-phenylpiperidino)ethyl]methylamine (2.24 g) in tetrahydrofuran (70 mL). The reaction was stirred at 23° C. for 18 hours. The reaction was evaporated to an oil, and the oil was partitioned between diethylether and 1N hydrochloric acid (100 mL). The organic layer was treated with etheral hydrochloric acid to produce the title compound as a white solid (950 mg); mp 230° C.; MS: m/z=633(M+1); NMR: 1.73 (m,2), 2.42 (m,1), 2.75 (m,1), 3.01 (s,4), 3.86 (m,4,), 4.43 (m,1), 4.85 (m,1), 5.34 (m,1), 7.34 (m,5), 7.73 (s 2), 7.87 (m,5), 8.06 (s,1), 11.36 (broad s,1). Analysis Calculated: C, 53.79; H, 4.36; N, 4.18; Found: C, 54.06; H, 4.48; N, 4.23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147083
Source datasetuspto-grants-2000_11
ORD IDord-433bf4565c334c36a5591d7b8492ab3e
Source noteuspto-grants-2000_11