4-Imidazolidinone, 1-[[1-(3-chloro-4-fluorophenyl)-5-(3-chloro-5-fluorophenyl)-1H-pyrazol-3-yl]carbonyl]- → HCID 58277272, 화합물

HRID 1949283노트

반응식

HRID 1949283 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[C:13]([C:14]3[CH:19]=[CH:18][C:17]([F:20])=[C:16]([Cl:21])[CH:15]=3)=[CH:12][C:11]([C:22](O)=[O:23])=[N:10]2)[CH:5]=[CH:6][C:7]=1[F:8].ClC1C=C(N2C(C3C=C(F)C=C(Cl)C=3)=CC(C([N:48]3[CH2:52][C:51](=[O:53])[NH:50][CH2:49]3)=O)=N2)C=CC=1F>>[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[C:13]([C:14]3[CH:19]=[CH:18][C:17]([F:20])=[C:16]([Cl:21])[CH:15]=3)=[CH:12][C:11]([C:22]([N:48]3[CH2:52][C:51](=[O:53])[NH:50][CH2:49]3)=[O:23])=[N:10]2)[CH:5]=[CH:6][C:7]=1[F:8]

참가 물질

3

실험 절차

The preparation of the title compound takes place starting from the compound of Example 75A in analogy to the synthesis of the compound of Example 1. 23 mg (39% of theory) of the title compound are obtained.

출처 및 근거

ORD 기록
ord-d95054bc80fc45fab8b8df955ae2fa0b
출처 데이터셋
uspto-grants-2013_03
특허 번호
US08399682B2

반응 노트

불러오는 중…