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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 737052생성일: 2026년 10월 24일

Triethylamine → 4-(3-Cyclohexyl-indole-1-sulfonyl)-N-(4-fluoro-benzyl)-benzamide

https://huagongshe.com/ko/reaction/737052

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-FluorobenzylamineHCID 67326—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물4-(3-Cyclohexyl-indole-1-sulfonyl)-benzoic acidHCID 58975217—
생성물4-(3-Cyclohexyl-indole-1-sulfonyl)-N-(4-fluoro-benzyl)-benzamideHCID 5897522499%

반응 단계

Add 4-Fluoro-benzylamine (72 mg, 0.574 mmol, 1.1 eq) followed by triethylamine (343 mg, 0.472 ml, 3.39 mmol, 6.5 eq) to a CH2CL2 solution (8 ml) of 4-(3-Cyclohexyl-indole-1-sulfonyl)-benzoic acid (200 mg, 0.521 mmol, 1 eq). Add benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (231 mg, 0.521 mmol, 1 eq) and stir at room temperature for 16 hours. Remove solvent on rotovap and purify crude by silica gel chromatography to give 4-(3-Cyclohexyl-indole-1-sulfonyl)-N-(4-fluoro-benzyl)-benzamide (232 mg, 99% yield). Mass Spectrum (m/e): 490.92 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07595339B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-c807b651e37d41dab9d061a614177513
출처 메모uspto-grants-2009_09