反応式
Br[C:2]1[CH:14]=[C:13]2[C:5]([C:6]3[C:7](=[O:23])[C:8]4[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:9]=4[C:10]([CH3:16])([CH3:15])[C:11]=3[NH:12]2)=[CH:4][CH:3]=1.COC1C=C2C(CCC(=O)C2(C)C)=CC=1.Cl.[Cl:40]C1C=C(NN)C=CC=1>>[Cl:40][C:2]1[CH:14]=[C:13]2[C:5]([C:6]3[C:7](=[O:23])[C:8]4[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:9]=4[C:10]([CH3:16])([CH3:15])[C:11]=3[NH:12]2)=[CH:4][CH:3]=1参加物
4
実験手順
Under the same conditions as the method for synthesizing Compound A3-1 and Compound A4, the title compound was prepared as a crude product from Compound A2 and (3-chlorophenyl)-hydrazine hydrochloric acid salt.
出典と根拠
- ORDレコード
- ord-f69f940b46e14520b60bf0f0c894ca5a
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09126931B2
関連ノート
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