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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7047생성일: 2026년 10월 24일

1-[4-(Bromomethyl)Phenyl]-1H-Pyrazole → cis-2-[(4-Chlorobenzenesulfonyl)-(4-pyrazol-1-yl-benzyl)-amino]-cycloheptanecarboxylic acid amide

https://huagongshe.com/ko/reaction/7047

반응식

참여 물질

역할이름HCID투입량
반응물1-[4-(Bromomethyl)Phenyl]-1H-PyrazoleHCID 2776479—
반응물cis-2-(4-Chlorobenzenesulfonylamino)-cycloheptanecarboxylic acid amideHCID 69656232—
생성물cis-2-[(4-Chlorobenzenesulfonyl)-(4-pyrazol-1-yl-benzyl)-amino]-cycloheptanecarboxylic acid amideHCID 6965556118%

반응 단계

The titled compound (40 mg) was prepared in 18% yield from cis-2-(4-chlorobenzenesulfonylamino)-cycloheptanecarboxylic acid amide (150 mg, 0.45 mmol) and 1-(4-bromomethyl-phenyl)-1H-pyrazole according to the N-alkylation procedure described in Example 11: 1H NMR (DMSO-d6) δ 8.46 (s, 1 H), 7.79 (d, 2 H, J=12.0 Hz), 7.71 (m, 3 H), 7.62 (d, 2 H, J=8.0 Hz), 7.40 (d, 2 H), J=8.0 Hz), 7.33 (s br, 1 H), 6.70 (s br, 1 H), 6.54 (s, 1 H), 4.56 (AB2,2 H,Δv=16,Jab=96 Hz), 4.00 (m, 1 H), 2.78 (m, 1 H), 2.30 (m, 1 H), 1.73 (m, 2 H), 1.37 (m, 7 H); MS m/e 509.12 (M+Na)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084178B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b44d5fef2bba4dd9be0b0a503504bc04
출처 메모uspto-grants-2006_08