돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1178939생성일: 2026년 10월 26일

Triethylamine → 4-(3-Chloro-indazole-1-sulfonyl)-N-(4-fluoro-benzyl)-benzamide

https://huagongshe.com/reaction/1178939

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Chloro-1H-indazoleHCID 95894—
반응물4-(4-Fluoro-benzylcarbamoyl)-benzenesulfonyl chlorideHCID 58975125—
용매DichloromethaneHCID 6344—
생성물4-(3-Chloro-indazole-1-sulfonyl)-N-(4-fluoro-benzyl)-benzamideHCID 5897515283%

반응 단계

Dissolve 3-chloro-1H-indazole (120 mg, 0.79 mmol) and 4-(4-fluoro-benzylcarbamoyl)-benzenesulfonyl chloride (114 mg, 0.35 mmol) in CH2Cl2 (2.0 mL) and treat with Et3N (50 L, 0.36 mmol). Stir the solution for 1 h at RT, then dilute with additional CH2Cl2 (20.0 mL) and wash with satd aq. NaHCO3 (15 mL). Dry, filter, and concentrate the organic phase and purify the crude material by flash chromatography (100% hexanes to 50% EtOAc/hexanes linear gradient) to give the title compound (129 mg, 83%) as a white foam. MS (ES+) 443.9 (M+1)+, (ES−) 442.0 (M−1)−. 1H NMR (400 MHz, CDCl3): δ 8.17 (d, 1H, J=8.3), 8.03 (d, 2H, J=8.2), 7.83 (d, 2H, J=8.9), 7.64 (m, 2H), 7.41 (t, 1H, J=7.4), 7.27 (m, 2H), 7.01 (t, 2H, J=8.9), 6.31 (br s, 1H), 4.57 (d, 2H, J=5.9).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07276516B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-33349d63e2504f7980b104abe6d22953
출처 메모uspto-grants-2007_10