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HRID 504615作成日:2026年10月25日

Ammonia → 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamide

https://huagongshe.com/reaction/504615

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Citric AcidHCID 311—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acidHCID 57475951—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamideHCID 5747595367%

反応条件

温度50 °C

反応手順

To a mixture of 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid (17.20 g), 1H-1,2,3-benzotriazol-1-ol (8.29 g) and N,N-dimethylformamide (150 ml) was added N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (11.8 g) at room temperature, and the mixture was stirred at 50° C. for 20 min. The mixture was allowed to cool to room temperature, and 28% aqueous ammonia (3.4 ml) was added. The reaction mixture was stirred at room temperature for 2 hr, and water was added. The mixture was acidified with 10% aqueous citric acid solution, and the resulting crystals were filtrated, washed with water, washed with cooled ethyl acetate, and dried to give the title compound (11.47 g, yield 67%) as colorless crystals. melting point 244-245° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07777047B2
出典データセットuspto-grants-2010_08
ORD IDord-5a405d98e7b94a328fc0c571cffa0677
出典メモuspto-grants-2010_08