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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1061340생성일: 2026년 10월 27일

N-Acetylsulfanilyl chloride → N-{4-[2-(1,4-Dioxa-8-aza-spiro[4.5]dec-8-yl)-phenylsulfamoyl]-phenyl]-acetamide

https://huagongshe.com/reaction/1061340

반응식

참여 물질

역할이름HCID투입량
반응물N-Acetylsulfanilyl chlorideHCID 8481—
반응물2-(1,4-Dioxa-8-aza-spiro[4.5]dec-8-yl)-phenylamine hydrochlorideHCID 22220431—
생성물N-{4-[2-(1,4-Dioxa-8-aza-spiro[4.5]dec-8-yl)-phenylsulfamoyl]-phenyl]-acetamideHCID 22220358—

반응 단계

The title compound was prepared from 2-(1,4-dioxa-8-aza-spiro[4.5]dec-8-yl)-phenylamine hydrochloride (which was obtained in Example 220) and N-acetylsulfanilyl chloride according to the procedure of Example 215 as a crystalline solid; 1H NMR (300 MHz, DMSO-d6) δ 1.73 (t, J=5.4 Hz, 4H), 2.73 (t, J=5.4 Hz, 4H), 3.33 (s, 4H), 3.89 (s, 3H), 7.00-7.10 (m, 2H), 7.10-7.20 (m, 1H), 7.30-7.40 (m, 1H), 7.67 (d, J=9.3 Hz, 2H), 7.71 (d, J=9.3 Hz, 2H), 8.79 (s, 1H), 10.29 (s, 1H); MS (ES) m/z: 432.2 (MH+); HRMS Calcd. for C21H26N3O5S (MH+): 432.1593. Found: 432.1597. Anal. Calcd. for C21N25N3O5S: C, 58.45; H, 5.84; N, 9.74. Found: C, 58.41; H, 5.83; N, 9.72.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06525202B2
출처 데이터셋uspto-grants-2003_02
ORD IDord-aeeb931724584f07a5c8df4c4bb3467b
출처 메모uspto-grants-2003_02