反応式
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:3]=1[C:4]([NH2:6])=[O:5].C(Cl)(=O)[C:13](Cl)=[O:14]>C(Cl)CCl>[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:3]=1[C:4]([N:6]=[C:13]=[O:14])=[O:5]参加物
4
実験手順
The title compound was prepared according to the procedure described in step-2 of Intermediate-8 by using 2-chloro-6-methylbenzamide (1.0 g, 5.9 mmol), oxalyl chloride (0.894 g, 7.1 mmol) and EDC (20 mL) to afford 1.00 g of the desired product.
後処理
- customThe title compound was prepared
出典と根拠
- ORDレコード
- ord-6ca60b71c0ef483e81bb004925663dd6
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09096545B2
関連ノート
読み込み中…