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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726823Generated: October 31, 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/726823

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-phenylpiperdino)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 ethereal 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 numberUS05710169
Source datasetuspto-grants-1998_01
ORD IDord-543b8f763f964c8b8c15205566346dfd
Source noteuspto-grants-1998_01