돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 381893생성일: 2026년 10월 25일

Ammonia → 2-(3-Chlorophenyl)-4-(4-fluorophenoxy)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone

https://huagongshe.com/reaction/381893

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물1-Bromo-3-chlorobenzeneHCID 7928—
반응물4-(4-fluorophenoxy)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinoneHCID 21934162—
용매WaterHCID 962—
생성물2-(3-Chlorophenyl)-4-(4-fluorophenoxy)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinoneHCID 10183726—

반응 단계

The title compound was prepared according to Example 93, substituting 1-bromo-3-chlorobenzene in place of 4-bromothioanisole and 4-(4-fluorophenoxy)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone (Example 108A) in place of 4-(4-fluorophenyl)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone (yield: 25 mg, 5.3%). mp 211-213° C. 1H NMR (300 MHz, DMSO-d6) δ 3.30 (s, 3H), 7.15 (d, J=9 Hz, 4H), 7.51-7.64 (m, 3H), 7.71-7.75 (m, 1H), 7.91 (d, J=9 Hz, 2H), 8.06 (d, J=9 Hz, 2H), 8.41 (s, 1H). MS (DCI/NH3) m/z 471 (M+H)+, 488 (M+NH4)+. Anal. calc. for C23H16ClFN2O4S.0.5 H2O: C, 57.62; H, 3.44; N, 5.85. Found: C, 57.62; H, 3.52; N, 5.48.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06307047B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-0a6032d26e6d4dc38b288e7d55135ec5
출처 메모uspto-grants-2001_10