反応式
N1(C2C=CC(CC3[C:12]([O:24]C)=NC4C(C=3Cl)=CC(Br)=CC=4C)=CC=2)C=CC=N1.[Cl:28][C:29]1[CH:34]=[CH:33][C:32]([C:35]([C:37]2[CH:38]=[C:39]3[C:44](=[CH:45][CH:46]=2)[N:43]=[C:42](Cl)[C:41]([CH2:48][C:49]2[CH:54]=[CH:53][C:52]([S:55]([CH3:58])(=[O:57])=[O:56])=[CH:51][CH:50]=2)=[C:40]3[Cl:59])=[O:36])=[CH:31][CH:30]=1.N1(C2C=CC(CC3C(OC)=NC4C(C=3Cl)=CC(Br)=CC=4)=CC=2)C=CC=N1>>[Cl:59][C:40]1[C:39]2[C:44](=[CH:45][CH:46]=[C:37]([C:35]([C:32]3[CH:33]=[CH:34][C:29]([Cl:28])=[CH:30][CH:31]=3)=[O:36])[CH:38]=2)[N:43]=[C:42]([O:24][CH3:12])[C:41]=1[CH2:48][C:49]1[CH:50]=[CH:51][C:52]([S:55]([CH3:58])(=[O:57])=[O:56])=[CH:53][CH:54]=1参加物
4
反応物 3
生成物 1
実験手順
The title compound was prepared by substituting 3-(4-(1H-pyrazol-1-yl)benzyl)-6-bromo-2,4-dichloroquinoline (Intermediate 6: step c) with (4-chlorophenyl)(2,4-dichloro-3-(4-(methylsulfonyl)benzyl)quinolin-6-yl)methanone (Intermediate 22: step a) then following the procedure described for the preparation of 3-(4-(1H-pyrazol-1-yl)benzyl)-6-bromo-4-chloro-2-methoxyquinoline (Intermediate 16).
出典と根拠
- ORDレコード
- ord-7fca3fa0efc54a148603269c84b79ceb
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09290476B2
関連ノート
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