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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852458Generated: November 2, 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/852458

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 numberUS07253157B2
Source datasetuspto-grants-2007_08
ORD IDord-a198bc86b6fe41e7a850da1020f04c9d
Source noteuspto-grants-2007_08