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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347688Generated: October 30, 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/347688

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 1151963670.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 0.21 g (0.44 mmol) 6′-chloro-2-methyl-[3,4′]bipyridinyl-3′-carboxylic acid (3,5-bis-trifluoromethyl-benzyl)-methyl-amide and 1.0 ml (9.0 mmol) 1-methylpiperazine was heated at 120° C. for 2 h. After cooling to room temperature the mixture was diluted with dichloromethane and washed with water. The aqueous layer was extracted with dichloromethane. The combined organic layers were dried over sodium sulfate and concentrated in vacuo to give 0.25 g of crude product. Flash chromatography gave 0.17 g (70%) of the title compound. MS m/e (%): 552 (M+H+, 100)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176205B2
Source datasetuspto-grants-2007_02
ORD IDord-0ea5e34bdcf54b28b7aafa3b3cb614d2
Source noteuspto-grants-2007_02