Dimethylamine → 2-Chloro-3-cyano-6-(N,N-dimethylamino)-4-methylpyridine
反応式
[CH3:1][NH:2][CH3:3].[C:4]([C:6]1[C:7]([Cl:14])=[N:8][C:9](Cl)=[CH:10][C:11]=1[CH3:12])#[N:5]>O1CCOCC1.C(OCC)(=O)C>[Cl:14][C:7]1[C:6]([C:4]#[N:5])=[C:11]([CH3:12])[CH:10]=[C:9]([N:2]([CH3:3])[CH3:1])[N:8]=1参加物
5
実験手順
Dimethylamine (8 mL) was added to a solution of 3-cyano-2,6-dichloro-4-methylpyridine (11.6 g) in dioxan (100 mL). After stirring for 2 hours the reaction mixture was diluted with ethyl acetate (1 L), washed with water, dried, filtered, and evaporated to a volume of 20 mL. The crystalline material was filtered to give 5.4 g of the title compound, suitable for use in the next reaction.
後処理
- washwashed with water
- customdried
- filtrationfiltered
- customevaporated to a volume of 20 mL
- filtrationThe crystalline material was filtered
出典と根拠
- ORDレコード
- ord-448e089b86694c728d60500d623cbf21
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05620974
反応ノート
読み込み中…