Ethyl orthoformate → 2-Cyanoethyl 4-(4-cyano-2-methoxyphenyl)-5-ethoxy-2,7-dimethyl-1,4-dihydro-1,6-naphthyridine-3-carboxylate
反応式
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[C:18]3[C:17](=[O:19])[NH:16][C:15]([CH3:20])=[CH:14][C:13]=3[NH:12][C:11]([CH3:21])=[C:10]2[C:22]([O:24][CH2:25][CH2:26][C:27]#[N:28])=[O:23])=[C:5]([O:29][CH3:30])[CH:4]=1)#[N:2].C(OCC)(OCC)O[CH2:33][CH3:34]>S(=O)(=O)(O)O>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[C:18]3[C:13](=[CH:14][C:15]([CH3:20])=[N:16][C:17]=3[O:19][CH2:33][CH3:34])[NH:12][C:11]([CH3:21])=[C:10]2[C:22]([O:24][CH2:25][CH2:26][C:27]#[N:28])=[O:23])=[C:5]([O:29][CH3:30])[CH:4]=1)#[N:2]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 130 °C
実験手順
1.52 g (3.76 mmol) of the compound from Example 25A are suspended in 40 ml of triethyl orthoformate and heated to 130° C. Then, over a total period of 8 hours, 10 drops of concentrated sulfuric acid are added each hour to the reaction mixture. It is then stirred at the same temperature overnight. After cooling, excess orthoester is removed in a rotary evaporator, and the crude product is purified by column chromatography (silica gel; mobile phase: cyclohexane/ethyl acetate 1:1). The product fractions are combined, the solvent is removed, and the residue is taken up in a little methanol. The crystallizing product is filtered off. Drying under high vacuum results in 1.09 g (67% of theory) of the title compound.
後処理
- temperatureAfter cooling
- customexcess orthoester is removed in a rotary evaporator
- customthe crude product is purified by column chromatography (silica gel; mobile phase: cyclohexane/ethyl acetate 1:1)
- customthe solvent is removed
- filtrationThe crystallizing product is filtered off
- customDrying under high vacuum
出典と根拠
- ORDレコード
- ord-1d97e194a69d4a30a0e5cec0694ca625
- 出典データセット
- uspto-grants-2013_05
- 特許番号
- US08436180B2
反応ノート
読み込み中…