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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1762817Erstellt: 25. Oktober 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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
Edukt1-(4-Fluorobenzyl)-2-chlorobenzimidazoleHCID 3020241—
LösungsmittelChloroformHCID 6212—
ProduktEthyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-YL]amino]piperidine-1-carboxylateHCID 301991640,5%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04835161
Quelldatensatzuspto-grants-1989_05
ORD IDord-4cf92ec6199f4e86980cc57881e512a1
Quellennotizuspto-grants-1989_05