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HRID 1372744作成日:2026年10月27日

Dimethylformamide → Methyl (3-chloro-4-((1-methyl-3-indazolylcarbonyl)amino)phenyl)acetate

https://huagongshe.com/reaction/1372744

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物1H-Indazole-3-carboxylic acid, 1-methyl-HCID 689105—
反応物Methyl 2-(4-amino-3-chlorophenyl)acetateHCID 13616273—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Methyl (3-chloro-4-((1-methyl-3-indazolylcarbonyl)amino)phenyl)acetateHCID 5877839389%

反応手順

To 1-methylindazole-3-carboxylic acid (600 mg, 3.41 mmol) and DMF (27.0 μl, 0.34 mmol) was added methylene chloride (20 ml). Under stirring at room temperature, oxalyl chloride (0.36 ml, 4.09 mmol) was added dropwise to the resulting mixture. After completion of the dropwise addition, the reaction mixture was stirred at room temperature for 50 hours and the solvent was distilled off under reduced pressure. The residue was dissolved in methylene chloride (5 ml). The resulting solution was added to a solution of methyl 4-amino-3-chlorophenylacetate (680 mg, 3.41 mmol) and triethylamine (1.42 ml, 10.2 mmol) in methylene chloride (5 ml) under stirring at room temperature. The reaction mixture was heated under reflux at room temperature for 7 hours. After the reaction mixture was cooled to room temperature, water was added thereto, followed by extraction with chloroform. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane-ethyl acetate (2:1, v/v) eluate fractions, methyl (3-chloro-4-((1-methyl-3-indazolylcarbonyl)amino)phenyl)acetate (1.08 g, 89%) was obtained as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07157487B2
出典データセットuspto-grants-2007_01
ORD IDord-e74ccd3037b044969bfe2b00997d3b10
出典メモuspto-grants-2007_01