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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017435Generated: October 30, 2026

2,2-Dimethyl-N-[6-(4-methyl-piperazin-1-yl)-4-o-tolyl-pyridin-3-yl]-propionamide → 6-(4-Methylpiperazin-1-yl)-4-(o-tolyl)pyridin-3-amine

https://huagongshe.com/reaction/1017435

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Dimethyl-N-[6-(4-methyl-piperazin-1-yl)-4-o-tolyl-pyridin-3-yl]-propionamideHCID 15887410—
SolventHydrochloric AcidHCID 313—
Product6-(4-Methylpiperazin-1-yl)-4-(o-tolyl)pyridin-3-amineHCID 1588741182%

Reaction Conditions

Temperature92.5 °C

Reaction Steps

A suspension of 56 g (152 mmol) 2,2-dimethyl-N-[6-(4-methyl-piperazin-1-yl)-4-o-tolyl-pyridin-3-yl]-propionamide in 1300 ml 3 N hydrochloric acid solution was heated to 90-95° C. overnight. The reaction mixture was cooled to room temperature, washed with three 500 ml portions diethyl ether and filtered over celite. The filtrate was diluted with 500 ml water and was adjusted to pH 7-8 by addition of 28% sodium hydroxide solution under ice cooling. The product was extracted with four 1000 ml portions of dichloromethane. The combined organic layers were washed with 500 ml brine, dried (magnesium sulfate) and evaporated to give 35 g (82%) of the title compound as a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479483B2
Source datasetuspto-grants-2002_11
ORD IDord-4978145d403b46cca64ee5e1ab372840
Source noteuspto-grants-2002_11