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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380754Generated: October 30, 2026

Ethyl Acetate → 3-Pyridinamine, N-methyl-4-(2-methylphenyl)-6-(4-methyl-1-piperazinyl)-

https://huagongshe.com/reaction/380754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl (6-(4-Methylpiperazin-1-yl)-4-(o-tolyl)pyridin-3-yl)carbaMateHCID 12167320—
ReactantRed-AlHCID 16684438—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product3-Pyridinamine, N-methyl-4-(2-methylphenyl)-6-(4-methyl-1-piperazinyl)-HCID 1588741289.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 0.5 g (1.4 mMol) [6-(4-methyl-piperazin-1-yl)-4-o-tolyl-pyridin-3-yl]-carbamic acid methyl ester in 3.0 ml dichloromethane was added over 10 minutes to a solution of 1.98 ml (6.9 mMol ) Red-Al® (70% in toluene) and 2.5 ml toluene (exothermic, cool with a water bath to avoid temperature to go >50° C.). The reaction mixture was stirred 2 hours at 50° C., cooled to 0° C., and 4 ml aqueous NaOH 1N were carefully (exothermic) added over 15 minutes, followed by 20 ml ethyl acetate. The phases were separated and the aqueous phase was extracted with ethyl acetate. The combined organic extracts were washed with deionized water and brine, dried (Na2SO4) and concentrated under reduced pressure to yield 0.37 g (89%) methyl-[6-(4-methyl-piperazin-1-yl)-4-o-tolyl-pyridin-3-yl]-amine as an orange resin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303790B1
Source datasetuspto-grants-2001_10
ORD IDord-5e223a1c91a34a1a9b3fb8e0add0c8a3
Source noteuspto-grants-2001_10