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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30236생성일: 2026년 10월 23일

3-Methylbenzaldehyde → 5-{1-[4-(3-Methyl-benzylamino)-phenyl]-ethylcarbamoyl}-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/30236

반응식

참여 물질

역할이름HCID투입량
반응물3-MethylbenzaldehydeHCID 12105—
반응물Ammonium ChlorideHCID 25517—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물5-[1-(4-Amino-phenyl)-ethylcarbamoyl]-thiophene-2-carboxylic acid methyl esterHCID 69135089—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물5-{1-[4-(3-Methyl-benzylamino)-phenyl]-ethylcarbamoyl}-thiophene-2-carboxylic acid methyl esterHCID 6913444943%

반응 단계

A mixture of 304.0 mg (1.0 mmol) 5-[1-(4-amino-phenyl)-ethylcarbamoyl]-thiophene-2-carboxylic acid methyl ester, 120.0 mg (1.0 mmol) m-tolualdehyde and 2 ml ethanol was heated under reflux for 1 h. The solvent was evaporated and 3 ml THF and 315 mg (5.0 mmol) sodium cyanoborohydride were added to the residue. After 18 h 5 ml aqueous ammonium chloride solution and 10 ml water were added. The aqueous phase was extracted with dichloromethane, the combined organic phases were dried over magnesium sulfate, the solvent was evaporated and the residue subjected to silica gel chromatography (ethyl acetate/petrol ether 1:1) to yield 175 mg (0.43 mmol) 5-{1-[4-(3-Methyl-benzylamino)-phenyl]-ethylcarbamoyl}-thiophene-2-carboxylic acid methyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423060B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-438e5106c59f43a0b80eee81d9de075a
출처 메모uspto-grants-2008_09