反応式
[CH3:1][O:2][C:3](=[O:18])[C:4]1[C:9]([NH:10][CH:11]([CH2:14][CH3:15])[CH2:12][CH3:13])=[CH:8][C:7]([CH3:16])=[N:6][C:5]=1Cl.[CH3:19][C:20]1[CH:28]=[CH:27][CH:26]=[CH:25][C:21]=1N(C)C.[C:29](=O)([O-])[O-].[K+].[K+].C[N:36]([CH:38]=O)C>[Cu]>[CH3:1][O:2][C:3](=[O:18])[C:4]1[C:9]([NH:10][CH:11]([CH2:14][CH3:15])[CH2:12][CH3:13])=[CH:8][C:7]([CH3:16])=[N:6][C:5]=1[NH:36][C:38]1[C:25]([CH3:21])=[CH:26][C:27]([CH3:29])=[CH:28][C:20]=1[CH3:19]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of 2-chloro-4-(1-ethyl-propylamino)-6-methyl-nicotinic acid methyl ester, trimethylaniline, potassium carbonate, copper in DMF was heated at reflux. The mixture was quenched with ammonium chloride and stirred for 20 min, filtered through celite and washed with ethyl acetate. The filtrate was extracted with ethyl acetate. The organic layer was separated, dried and concentrated to dryness. The residue was purified through silica gel column chromatography using 2% methanol in chloroform as eluent to give the title compound as a solid.
後処理
- temperaturewas heated
- temperatureat reflux
- customThe mixture was quenched with ammonium chloride
- filtrationfiltered through celite
- washwashed with ethyl acetate
- extractionThe filtrate was extracted with ethyl acetate
- customThe organic layer was separated
- customdried
- concentrationconcentrated to dryness
- customThe residue was purified through silica gel column chromatography
出典と根拠
- ORDレコード
- ord-4f03e17beaa84580b5c35b5b6b64d128
- 出典データセット
- uspto-grants-2006_10
- 特許番号
- US07125880B1
関連ノート
読み込み中…