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HRID 2235077作成日:2026年10月27日

Ammonium Hydroxide → 2-chloro-4-[(2,3-dihydro-1H-indole-6-carbonyl)-amino]-benzoic acid methyl ester

https://huagongshe.com/reaction/2235077

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物2-chloro-4-[(1H-indole-6-carbonyl)-amino]-benzoic acid methyl esterHCID 68697374—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-chloro-4-[(2,3-dihydro-1H-indole-6-carbonyl)-amino]-benzoic acid methyl esterHCID 68698445—

反応条件

温度0 °C

反応手順

Sodium cyanoborohydride (2.6 g, 41.6 mmol, 3 equiv.) was added to a stirred solution of 2-chloro-4-[(1H-indole-6-carbonyl)-amino]-benzoic acid methyl ester (1.4 g, 4.2 mmol, 1 equiv.) in acetic acid (25 mL) over 5 minutes at room temperature. The mixture was stirred for 30 minutes then cooled to 0° C. and poured onto concentrated ammonium hydroxide (78 mL, d=0.880) at 0° C. The mixture was diluted with water (25 mL) and dichloromethane (25 mL), the organic layer was separated and the aqueous layer extracted with dichloromethane (2×25 mL). The combined organic layers were dried over Na2SO4 and the solvent removed under vacuum to afford crude 2-chloro-4-[(2,3-dihydro-1H-indole-6-carbonyl)-amino]-benzoic acid methyl ester, 0.75 g, this material was taken onto the next step without further purification. LC @215 nm; Rt 1.04: 71%, m/z (ES+): 331 (M+H+.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07713996B2
出典データセットuspto-grants-2010_05
ORD IDord-3677983030114d40a78d540af3723026
出典メモuspto-grants-2010_05