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HRID 1994789作成日:2026年10月25日

2-Trifluoromethylbenzenesulphonyl chloride → ethyl 7-({[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1994789

反応式

関与物質

役割名称HCID仕込み量
反応物2-Trifluoromethylbenzenesulphonyl chlorideHCID 136616—
反応物1H-Indole-2-carboxylic acid, 7-amino-, ethyl esterHCID 11138194—
溶媒PyridineHCID 1049—
生成物ethyl 7-({[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylateHCID 5747617888.2%

反応手順

To a mixture of ethyl 7-amino-1H-indole-2-carboxylate (4.1 g) and pyridine (60 mL) was added 2-trifluoromethylbenzenesulfonyl chloride (5.0 g) under ice-cooling, and the mixture was stirred from under ice-cooling to room temperature for 18 hr. The reaction mixture was concentrated, and the residue was diluted with ethyl acetate. The solution was washed with aqueous citric acid solution and saturated brine, and filtrated through silica gel. The eluate was concentrated under reduced pressure, and the obtained pale-brown oil was crystallized from ethyl acetate-hexane to give the title compound (7.3 g, yield 88%) as pale-brown crystals. MS: 413 (MH+). melting point: 138-139° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07652133B2
出典データセットuspto-grants-2010_01
ORD IDord-1610d74c26854347b0a5242d28f25b99
出典メモuspto-grants-2010_01