Acetyl chloride → N-(5,6-dichloropyridin-3-yl)acetamide
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([NH2:9])[CH:5]=[N:6][C:7]=1[Cl:8].C(N(CC)CC)C.[C:17](Cl)(=[O:19])[CH3:18]>C(Cl)Cl>[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][C:17](=[O:19])[CH3:18])[CH:5]=[N:6][C:7]=1[Cl:8]参加物
5
実験手順
To a stirred solution of 5,6-dichloropyridin-3-amine (commercially available) and triethyl amine (3 eq) in CH2Cl2 (0.2 M) at 0° C. was added acetyl chloride (2 eq). After stirring at room temperature overnight the reaction mixture was concentrated under vacuum and the resulting crude residue was purified by chromatography (silica gel, 20-50% EtOAc in hexanes) to afford N-(5,6-dichloropyridin-3-yl)acetamide.
後処理
- concentrationwas concentrated under vacuum
- customthe resulting crude residue was purified by chromatography (silica gel, 20-50% EtOAc in hexanes)
出典と根拠
- ORDレコード
- ord-aaabcfc7ad9e4be791a971b3247d9d04
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08895577B2
反応ノート
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