Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762817Generated: October 26, 2026

Ethyl 4-amino-1-piperidinecarboxylate → Ethyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-YL]amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/1762817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
Reactant1-(4-Fluorobenzyl)-2-chlorobenzimidazoleHCID 3020241—
SolventChloroformHCID 6212—
ProductEthyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-YL]amino]piperidine-1-carboxylateHCID 301991640.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 9.8 parts of ethyl 4-amino-1-piperidinecarboxylate and 15 parts of 2-chloro-1-(4-fluorophenylmethyl)-1H-benzimidazole was heated to 120° C. The mixture was stirred at 120° C. during 43 hours. After cooling, 100 parts of trichloromethane were added and the whole was thouroughly stirred. The mixture was washed with water. The aqueous layer was separated and the organic mixture was filtered and evaporated. The collected solid material was dissolved in 100 parts of water and subsequently 100 parts of 20% sodium hydroxide solution were added. The precipitate was filtered and dried in vacuo at 50° C., yielding 12.1 parts (40.5%) of ethyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinecarboxylate; mp. 181° C. (compound 21).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835161
Source datasetuspto-grants-1989_05
ORD IDord-4cf92ec6199f4e86980cc57881e512a1
Source noteuspto-grants-1989_05