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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2235076생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2235076

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1H-indole-6-carboxylic acidHCID 595230—
반응물PyBroPHCID 2733179—
반응물Methyl 4-Amino-2-chlorobenzoateHCID 11839197—
용매TetrahydrofuranHCID 8028—
생성물2-chloro-4-[(1H-indole-6-carbonyl)-amino]-benzoic acid methyl esterHCID 6869737426%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07713996B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-f6120e17224a4b6085e2cad556988c9b
출처 메모uspto-grants-2010_05