4-Imidazolidinone, 1-[[1-(3-chloro-4-fluorophenyl)-5-(3-chloro-5-fluorophenyl)-1H-pyrazol-3-yl]carbonyl]- → HCID 44230125, 화합물

HRID 1949281노트

반응식

HRID 1949281 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([N:8]2[C:12]([C:13]3[CH:18]=[C:17]([F:19])[CH:16]=[C:15]([F:20])[CH:14]=3)=[CH:11][C:10]([C:21]([OH:23])=O)=[N:9]2)[CH:5]=[CH:6][CH:7]=1.ClC1C=C(N2C(C3C=C(F)C=C(Cl)C=3)=CC(C([N:47]3[CH2:51][C:50](=[O:52])[NH:49][CH2:48]3)=O)=N2)C=CC=1F>>[Cl:1][C:2]1[CH:3]=[C:4]([N:8]2[C:12]([C:13]3[CH:14]=[C:15]([F:20])[CH:16]=[C:17]([F:19])[CH:18]=3)=[CH:11][C:10]([C:21]([N:47]3[CH2:51][C:50](=[O:52])[NH:49][CH2:48]3)=[O:23])=[N:9]2)[CH:5]=[CH:6][CH:7]=1

참가 물질

3

반응물 2

HCID 442301814-Imidazolidinone, 1-[[1-(3-chloro-4-fluorophenyl)-5-(3-chloro-5-fluorophenyl)-1H-pyrazol-3-yl]carbonyl]-HCID 58277362HCID 58277362, 화합물

생성물 1

HCID 44230125HCID 44230125, 화합물

실험 절차

The preparation of the title compound takes place starting from the compound of Example 73A in analogy to the synthesis of the compound of Example 1. 28 mg (73% of theory) of the title compound are obtained.

출처 및 근거

ORD 기록
ord-f921749075684c1b98b7c006933bc8eb
출처 데이터셋
uspto-grants-2013_03
특허 번호
US08399682B2

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