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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375945Generated: November 1, 2026

[1,1'-Biphenyl]-2-carbonyl chloride → N-[4-[1,2,3,6-tetrahydro-1-(phenylmethyl)-4-pyridinyl]phenyl]-[1,1'-biphenyl]-2-carboxamide

https://huagongshe.com/reaction/1375945

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[1,1'-Biphenyl]-2-carbonyl chlorideHCID 12563768—
Reactant4-[1,2,3,6-Tetrahydro-1-(phenylmethyl)-4-pyridinyl]benzenamineHCID 22499416—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductN-[4-[1,2,3,6-tetrahydro-1-(phenylmethyl)-4-pyridinyl]phenyl]-[1,1'-biphenyl]-2-carboxamideHCID 2249938192.5%

Reaction Steps

[1,1′-Biphenyl]-2-carbonyl chloride (0.05 mole) was added dropwise to a stirring mixture of 4-[1,2,3,6-tetrahydro-1-(phenylmethyl)-4-pyridinyl]benzenamine (0.045 mole) in THF (300 ml) and triethylamine (25 ml). The mixture was stirred overnight. The solvent was evaporated. The residue was dissolved in DCM. The organic layer was'separated, washed, dried, filtered and the solvent was evaporated. The residue was triturated in DIPE. The precipitate was filtered off and dried, yielding 18.5 g of N-[4-[1,2,3,6-tetrahydro-1-(phenylmethyl)-4-pyridinyl]phenyl]-[1,1′-biphenyl]-2-carboxamide (intermediate 11, melting point 142° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169796B2
Source datasetuspto-grants-2007_01
ORD IDord-805bb22685e4417e9bbd3fdfa00dbf00
Source noteuspto-grants-2007_01