反応式
C(=O)([O-])[O-].[K+].[K+].[C:7]1(=O)[O:11][CH2:10][CH2:9][O:8]1.[C:13]1([C:23]2[N:28]=[N:27][N:26]=[C:25]([C:29]3[CH:34]=[CH:33]C(O)=[CH:31][C:30]=3[OH:36])[C:24]=2[C:37]2[C:46]3[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=3)[CH:40]=[CH:39][CH:38]=2)[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][CH:14]=1>CN(C=O)C>[C:13]1([C:23]2[N:28]=[N:27][N:26]=[C:25]([C:29]3[CH:34]=[CH:33][C:7]([O:11][CH2:10][CH2:9][OH:8])=[CH:31][C:30]=3[OH:36])[C:24]=2[C:37]2[C:46]3[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=3)[CH:40]=[CH:39][CH:38]=2)[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][CH:14]=1参加物
5
反応条件
- 温度
- 140 °C
実験手順
9.39 g of potassium carbonate and 4.39 g of ethylene carbonate are added to 20 g of the product from Example A6 in 200 ml of anhydrous DMF. The reaction mixture is heated at 140° C. for 18 h. The salts which precipitate are filtered off and washed with toluene. The combined organic phase is freed of solvent in vac. and used directly for the further reaction.
後処理
- filtrationThe salts which precipitate are filtered off
- washwashed with toluene
- customand used directly for the further reaction
出典と根拠
- ORDレコード
- ord-5ff40fbc24cd473c904d9efe22b51f9b
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07087753B2
関連ノート
読み込み中…