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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288321Generated: October 26, 2026

Imidazolate → Methyl 5-[2-(4-cyanophenyl)ethylcarbonylamino]-6-methylamino-nicotinate

https://huagongshe.com/reaction/2288321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazolateHCID 3386966—
Reactant3-(4-Cyanophenyl)-propionic acidHCID 9361742—
ReactantMethyl 5-amino-6-(methylamino)pyridine-3-carboxylateHCID 18412673—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-[2-(4-cyanophenyl)ethylcarbonylamino]-6-methylamino-nicotinateHCID 18412623—

Reaction Steps

A solution of 2.6 g (15 mMol) of 3-(4-cyanophenyl)propionic acid in 25 ml of absolute tetrahydrofuran was mixed with 2.4 g (15 mMol) of N,N'-carbonyldiimidazole and stirred for 20 minutes at room temperature. Then the imidazolide was mixed with a solution of 2.3 g (13 mMol) of methyl 5-amino-6-methylamino-nicotinate in 25 ml of dimethylformamide and heated for 3 hours to 100° C. After the removal of the solvent in vacuo the crude product obtained was taken up in ethyl acetate, the organic phase was washed with water and after drying over sodium sulphate it was again freed from solvent. The residue obtained was purified by flash chromatography (silica gel; gradient: dichloromethane to dichloromethane/ethanol=19:1). Yield: 2.1 g (50% of theory) of beige solid Rf value: 0.54 (silica gel; ethyl acetate/ethanol/ammonia=90:10:1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087380
Source datasetuspto-grants-2000_07
ORD IDord-92c9897b334a458ea7001babe9ecab4e
Source noteuspto-grants-2000_07