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HRID 2235078생성일: 2026년 10월 27일

Pyridine → 2-chloro-4-{[1-(3-chloro-benzenesulfonyl)-2,3-dihydro-1H-indole-6-carbonyl]-amino}-benzoic acid methyl ester

https://huagongshe.com/reaction/2235078

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물3-Chlorobenzenesulphonyl chlorideHCID 17909—
반응물2-chloro-4-[(2,3-dihydro-1H-indole-6-carbonyl)-amino]-benzoic acid methyl esterHCID 68698445—
용매DichloromethaneHCID 6344—
생성물2-chloro-4-{[1-(3-chloro-benzenesulfonyl)-2,3-dihydro-1H-indole-6-carbonyl]-amino}-benzoic acid methyl esterHCID 68696120—

반응 단계

3-Chlorobenzenesulphonyl chloride (71 mg, 0.3 mmol, 1.1 equiv.) was added to a mixture of crude 2-chloro-4-[(2,3-dihydro-1H-indole-6-carbonyl)-amino]-benzoic acid methyl ester (100 mg, 0.3 mmol, 1 equiv.) and pyridine (0.2 mL, 2.4 mmol, 8 equiv.) in dichloromethane (2 ml) and the mixture was stirred at room temperature for 16 hours. The solvent was removed under a stream of N2 and the residue purified by column chromatography (SiO2, dichloromethane). The fractions were combined to afford crude 2-chloro-4-{[1-(3-chloro-benzenesulfonyl)-2,3-dihydro-1H-indole-6-carbonyl]-amino}-benzoic acid methyl ester, 101 mg. This material was taken onto the next step without further purification. LC @215 nm; Rt 2.52: 84%, m/z (ES+): 505 (M+H+.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07713996B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-a6ca3900af214f7893f1f298564e0097
출처 메모uspto-grants-2010_05