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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2073802생성일: 2026년 10월 26일

Methyl chloroformate → 2-Amino-3-(2-methyl-6-methoxycarbonylaminobenzylideneamino)pyridine

https://huagongshe.com/reaction/2073802

반응식

참여 물질

역할이름HCID투입량
반응물Methyl chloroformateHCID 6586—
반응물2,3-DiaminopyridineHCID 9956—
반응물2-Methyl-6-methoxycarbonylaminobenzaldehydeHCID 14499823—
반응물2-Amino-6-methylbenzaldehydeHCID 23046538—
촉매Titanium TetrachlorideHCID 24193—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물2-Amino-3-(2-methyl-6-methoxycarbonylaminobenzylideneamino)pyridineHCID 1449982419.6%

반응 단계

To a solution of 2,3-diaminopyridine (546 mg) and 2-methyl-6-methoxycarbonylaminobenzaldehyde (966 mg)*, which was prepared by reacting 2-methyl-6-aminobenzaldehyde with methyl chloroformate according to a similar manner to that of Preparation 2, and triethylamine (2.5 g) in methylene chloride (26 ml) was added a 0.5M solution of titanium tetrachloride in methylene chloride (6 ml) at 0° C. and the mixture was stirred for 2 hours at the same temperature. To the mixture, water was added and the insoluble materials were removed by filtration, and the organic layer was separated. The solvent was evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel (27 g), eluting with a mixture of chloroform and methanol (50:1). The fractions containing the desired product were combined and the solvent was removed under reduced pressure. The residue was triturated with diethyl ether to give 2-amino-3-(2-methyl-6-methoxycarbonylaminobenzylideneamino)pyridine (279 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04920129
출처 데이터셋uspto-grants-1990_04
ORD IDord-0170d304173d4fbaaa3ebafe0360ad10
출처 메모uspto-grants-1990_04