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HRID 2235076作成日:2026年10月27日

Diisopropylethylamine → 2-chloro-4-[(1H-indole-6-carbonyl)-amino]-benzoic acid methyl ester

https://huagongshe.com/reaction/2235076

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1H-indole-6-carboxylic acidHCID 595230—
反応物PyBroPHCID 2733179—
反応物Methyl 4-Amino-2-chlorobenzoateHCID 11839197—
溶媒TetrahydrofuranHCID 8028—
生成物2-chloro-4-[(1H-indole-6-carbonyl)-amino]-benzoic acid methyl esterHCID 6869737426%

反応手順

Bromo-tris-pyrrolidino-phosphonium hexafluorophosphate (8.3 g, 17.8 mmol, 1.1 equiv.) and diisopropyl ethyl amine (4.4 ml, 33.9 mmol, 2.1 equiv.) were added to 1H-indole-6-carboxylic acid (2.6 g, 16.2 mmol, 1 equiv.) in tetrahydrofuran (30 mL) and the mixture was shaken for 5 minutes at room temperature. 4-Amino-2-chlorobenzoic acid methyl ester (3.3 g, 17.9 mmol, 1.1 equiv.) was added and the resultant mixture was shaken at room temperature for 16 hours. The solvent was removed under vacuum and the residue triturated with dichloromethane (10 mL). The solid was filtered to afford 2-chloro-4-[(1H-indole-6-carbonyl)-amino]-benzoic acid methyl ester, 1.4 g (26% yield). LC @215 nm; Rt 1.36: 90%, m/z (ES+): 329 (M+H+.); δH (400 MHz; d6-DMSO) 11.65 (1H, s), 10.59 (1H, s), 8.16 (1H, s), 8.10 (1H, s), 7.93 (2H, m), 7.65 (2H, s), 7.59 (1H, m), 6.62 (1H, s), 3.85 (3H, s).

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-f6120e17224a4b6085e2cad556988c9b
出典メモuspto-grants-2010_05