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HRID 2073802作成日:2026年10月26日

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

https://huagongshe.com/reaction/2073802

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl chloroformateHCID 6586—
反応物2,3-DiaminopyridineHCID 9956—
反応物2-Methyl-6-methoxycarbonylaminobenzaldehydeHCID 14499823—
反応物2-Amino-6-methylbenzaldehydeHCID 23046538—
触媒Titanium TetrachlorideHCID 24193—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物2-Amino-3-(2-methyl-6-methoxycarbonylaminobenzylideneamino)pyridineHCID 1449982419.6%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04920129
出典データセットuspto-grants-1990_04
ORD IDord-0170d304173d4fbaaa3ebafe0360ad10
出典メモuspto-grants-1990_04