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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190561Generated: October 26, 2026

6-chloro-N-(3-iodo-4-methyl-phenyl)-nicotinamide → 4-(3-Trifluoromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid (3-iodo-4-methyl-phenyl)-amide

https://huagongshe.com/reaction/2190561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-chloro-N-(3-iodo-4-methyl-phenyl)-nicotinamideHCID 7925562—
ReactantN-(3-Iodo-4-methyl-phenyl)-6-morpholin-4-yl-nicotinamideHCID 17541675—
Reactant4-(3-Trifluoromethylphenyl)piperidine, HClHCID 22252849—
Product4-(3-Trifluoromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid (3-iodo-4-methyl-phenyl)-amideHCID 59318060—

Reaction Steps

4-(3-Trifluoromethyl-phenyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-5′-carboxylic acid (3-iodo-4-methyl-phenyl)-amide was prepared from 6-chloro-N-(3-iodo-4-methyl-phenyl)-nicotinamide and 4-(3 trifluoromethyl-phenyl)piperidine hydrochloride in a manner similar to the one described in the synthesis of N-(3-iodo-4-methyl-phenyl)-6-morpholin-4-yl-nicotinamide above. The product was isolated after silica gel column purification with 20-40% EtOAc in hexanes. HRMS m/z calcd for C25H23N3OF3I [M+H]+: 566.0911. Found: 566.0910. START

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-cfcb7610897c4515acab137c224fb25d
Source noteuspto-grants-2012_12