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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28680생성일: 2026년 10월 23일

Benzoyl chloride → N-(6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-yl)benzamide

https://huagongshe.com/ko/reaction/28680

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chlorideHCID 7412—
반응물DiisopropylethylamineHCID 81531—
반응물6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amineHCID 597879—
용매DichloromethaneHCID 6344—
생성물N-(6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-yl)benzamideHCID 1140602326%

반응 단계

To a solution of 6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amine (50 mg, 0.19 mmol) and benzoyl chloride (24 μL, 0.21 mmol) in dichloromethane (1 mL) at 0° C. was added diisopropylethylamine (66 μL, 0.38 mmol). The mixture was stirred at room temperature 15 hours, the solvent removed, and the residue purified by flash chromatography (0-30% ethyl acetate-hexanes) to give 18 mg (26% yield) of a yellow solid. 1H-NMR (CDCl3): δ 8.97 (s, 1H), 7.78 (d, 2H), 7.61 (m, 1H), 7.52 (m, 1H), 7.44 (t, 2H), 7.23 (m, 1H), 7.17 (d, 1H), 6.42 (d, 1H), 5.34 (m, 1H), 2.72 (m, 2H), 2.32 (m, 1H), 2.02-1.93 (m, 3H); MS m/z 369 (M−1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419997B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-b49dcf9f9b4249aaba23456d368fe08c
출처 메모uspto-grants-2008_09