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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375953Generated: November 1, 2026

1-Chloroethyl chloroformate → N-[4-(1,2,3,6-tetrahydro-4-pyridinyl)phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamide

https://huagongshe.com/reaction/1375953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantN-[4-[1,2,3,6-tetrahydro-1-(phenylmethyl)-4-pyridinyl]phenyl]-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-carboxamideHCID 22499387—
Solvent1,2-DichloroethaneHCID 11—
ProductN-[4-(1,2,3,6-tetrahydro-4-pyridinyl)phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamideHCID 22499395126.2%

Reaction Steps

1-Chloroethyl chloroformate (0.078 mol) was added dropwise to a stirring mixture of intermediate (20) (0.039 mol) in 1,2-dichloro-ethane (500 ml). The mixture was stirred for 30 minutes and then stirred and refluxed overnight. The solvent was evaporated. Methanol (500 ml) was added. The mixture was stirred and refluxed overnight. The solvent was evaporated. The residue was triturated in DIPE. The precipitate was filtered off and dried, yielding 20.8 g of N-[4-(1,2,3,6-tetrahydro-4-pyridinyl)phenyl]-4′-(trifluoro-methyl )-[1,1′-biphenyl]-2-carboxamide (intermediate 21).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169796B2
Source datasetuspto-grants-2007_01
ORD IDord-644646099f2f46b186fda1e8baa8895f
Source noteuspto-grants-2007_01