反応式
[CH2:1]([NH:3][CH2:4][CH3:5])[CH3:2].[CH2:6]([O:8][C:9]([C:11]1[N:12]=[N:13][C:14]([Cl:18])=[CH:15][C:16]=1Cl)=[O:10])[CH3:7]>C(OCC)(=O)C>[CH2:6]([O:8][C:9]([C:11]1[N:12]=[N:13][C:14]([Cl:18])=[CH:15][C:16]=1[N:3]([CH2:4][CH3:5])[CH2:1][CH3:2])=[O:10])[CH3:7]参加物
4
実験手順
Diethylamine (86 mg, 1.3 equivalents, 1.2 mmol) is added to a solution of 4,6-dichloro-pyridazine-3-carboxylic acid ethyl ester (0.2 g, 0.91 mmol) in ethyl acetate (10 mL) at room temperature. After overnight stirring, the reaction is quenched with water (6 mL). The organic layer is separated and the aqueous layer extracted (2×15 mL) with ethyl acetate. The combined organic layers are dried and solvent removed to give 230 mg of 6-chloro-4-diethylamino-pyridazine-3-carboxylic acid ethyl ester as a yellowish oil.
後処理
- customthe reaction is quenched with water (6 mL)
- customThe organic layer is separated
- extractionthe aqueous layer extracted (2×15 mL) with ethyl acetate
- customThe combined organic layers are dried
- customsolvent removed
出典と根拠
- ORDレコード
- ord-9e8b97256656485b83fc086a99a545bc
- 出典データセット
- uspto-grants-2006_10
- 特許番号
- US07122546B2
関連ノート
読み込み中…