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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50191생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/50191

반응식

참여 물질

역할이름HCID투입량
반응물ImidazolateHCID 3386966—
반응물3-(4-Cyanophenyl)-propionic acidHCID 9361742—
반응물Methyl 5-amino-6-(methylamino)pyridine-3-carboxylateHCID 18412673—
용매TetrahydrofuranHCID 8028—
생성물Methyl 5-[2-(4-cyanophenyl)ethylcarbonylamino]-6-methylamino-nicotinateHCID 18412623—

반응 단계

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-methylaminonicotinate in 25 mL of dimethyfformamide 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 sulfate 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710055B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-8ed547a2fc2a4ce58ab475f72df20328
출처 메모uspto-grants-2004_03