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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347679Generated: October 29, 2026

1-Methylpiperazine → 2-Methyl-6'-(4-methyl-piperazin-1-yl)-[3,4']bipyridinyl-3'-carboxylic acid (3,5-bis-trifluoromethyl-benzyl)-methyl-amide

https://huagongshe.com/reaction/347679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant6'-Chloro-2-methyl-[3,4']bipyridinyl-3'-carboxylic acid (3,5-bis-trifluoromethyl-benzyl)-methyl-amideHCID 58694595—
SolventDichloromethaneHCID 6344—
Product2-Methyl-6'-(4-methyl-piperazin-1-yl)-[3,4']bipyridinyl-3'-carboxylic acid (3,5-bis-trifluoromethyl-benzyl)-methyl-amideHCID 11519636—

Reaction Conditions

Temperature120 °C

Reaction Steps

In accordance with process variant a) a mixture of 6′-chloro-2-methyl-[3,4′]bipyridinyl-3′-carboxylic acid (3,5-bis-trifluoromethyl-benzyl)-methyl-amide and 1-methylpiperazine is heated at about 120° C. for 2 h. After cooling to room temperature, the mixture is diluted with dichloromethane and washed with water. The aqueous layer is worked up in conventional manner to give the compound 2-methyl-6′-(4-methyl-piperazin-1-yl)-[3,4′]bipyridinyl-3′-carboxylic acid (3,5-bis-trifluoromethyl-benzyl)-methyl-amide of formula I-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176205B2
Source datasetuspto-grants-2007_02
ORD IDord-2c372eb730404ae9ab97ad43217bb44a
Source noteuspto-grants-2007_02