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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190536Generated: November 4, 2026

6-Chloronicotinoyl Chloride → 6-Chloro-N-(3,2',4'-trifluoro-biphenyl-4-yl)-nicotinamide

https://huagongshe.com/reaction/2190536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloronicotinoyl ChlorideHCID 2782165—
Reactant6-chloro-N-(4-iodo-3-methyl-phenyl)-nicotinamideHCID 59318138—
Reactant3,2',4'-Trifluoro-biphenyl-4-ylamineHCID 59318163—
SolventEthyl AcetateHCID 8857—
Product6-Chloro-N-(3,2',4'-trifluoro-biphenyl-4-yl)-nicotinamideHCID 59318055—

Reaction Steps

6-Chloro-N-(3,2′,4′-trifluoro-biphenyl-4-yl)-nicotinamide was prepared from 3,2′,4′-trifluoro-biphenyl-4-yl amine and 6-chloronicotinoyl chloride following a procedure similar to the one described in the synthesis of 6-chloro-N-(4-iodo-3-methyl-phenyl)-nicotinamide, above. The product was isolated after a silica gel column chromatography with 0-30% EtOAc in hexanes. H1 NMR (300 MHz, chloroform-d) d ppm 6.91 (m, 2H), 7.15 (apparent t, J=8.1 Hz, 1H), 7.24-7.1 (m, 3H), 7.95 (dd, J=10.5 8.1 Hz, 2H), 8.69 (d, J=2.1 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-a84197496ab44f699decf74b13cfd7ee
Source noteuspto-grants-2012_12