反応式
[CH2:1](N1C=C2C(C=C(Br)C=C2)=N1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:18][C:19]1[CH:27]=[C:26]2[C:22]([CH:23]=[N:24][NH:25]2)=[CH:21][C:20]=1[F:28]>>[CH2:1]([N:24]1[CH:23]=[C:22]2[C:26]([CH:27]=[C:19]([Cl:18])[C:20]([F:28])=[CH:21]2)=[N:25]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
3
実験手順
This compound was prepared in a manner similar to the procedure described for the preparation of 2-benzyl-6-bromo-2H-indazole, using 6-chloro-5-fluoro-1H-indazole in place of 6-bromoindazole. 1H-NMR (300 MHz, DMSO-d6) 8.54 (s, 1H), 7.90 (d, 1H), 7.71 (d, 1H), 7.36 to 7.29 (m, 5H), 5.64 (s, 2H); ES-MS m/z 261.0 [M+H]+, RT (min) 3.56.
後処理
- customThis compound was prepared in a manner similar to the procedure
- customES-MS m/z 261.0 [M+H]+, RT (min) 3.56
出典と根拠
- ORDレコード
- ord-08504bf612ff4d49958303b44747c49d
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08431695B2
関連ノート
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