戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1960254作成日:2026年10月27日

1-Hydroxybenzotriazole → ethyl [2-({7-[methyl(2-thienylsulfonyl)amino]-1H-indol-2-yl}carbonyl)hydrazino](oxo)acetate

https://huagongshe.com/reaction/1960254

反応式

関与物質

役割名称HCID仕込み量
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物Ethyl 2-hydrazinyl-2-oxoacetateHCID 2786935—
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ethyl [2-({7-[methyl(2-thienylsulfonyl)amino]-1H-indol-2-yl}carbonyl)hydrazino](oxo)acetateHCID 5913560764.2%

反応手順

To a mixture of 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid (0.50 g), 1H-1,2,3-benzotriazol-1-ol (0.24 g) and N,N-dimethylformamide (10 ml) was added N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (0.30 g) at room temperature, and the mixture was stirred for 10 min. Ethyl hydrazino(oxo)acetate (0.33 g) was added, and the reaction mixture was stirred at room temperature for 2 hr. Water was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography to give the title compound (0.43 g, yield 63%) as colorless crystals from a fraction eluted with ethyl acetate. melting point 133-134° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08410087B2
出典データセットuspto-grants-2013_04
ORD IDord-4c193a3edbf54b0fb215d9db291010f4
出典メモuspto-grants-2013_04