反応式
C([O:8][C:9]1[CH:10]=[C:11]([C:15]2[N:20]=[C:19]([NH:21][S:22]([C:25]3[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][N:26]=3)(=[O:24])=[O:23])[C:18]([O:32][C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=3[O:39][CH3:40])=[C:17]([O:41][CH3:42])[N:16]=2)[CH:12]=[CH:13][CH:14]=1)C1C=CC=CC=1.C(O)C.C1CCC=CC=1>O1CCOCC1.[Pd]>[OH:8][C:9]1[CH:10]=[C:11]([C:15]2[N:20]=[C:19]([NH:21][S:22]([C:25]3[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][N:26]=3)(=[O:24])=[O:23])[C:18]([O:32][C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=3[O:39][CH3:40])=[C:17]([O:41][CH3:42])[N:16]=2)[CH:12]=[CH:13][CH:14]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
1.46 g of 5-methyl-pyridine-2-sulfonic acid [2-(3-benzyloxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide were dissolved in dioxane (25 ml) by gentle warming than ethanol (50 ml) was added followed by cyclohexadiene (6 g) and palladium on charcoal, 10%, (1.46 g). The solution was refluxed for 20 h, the catalyst removed by filtration and the solution concentrated on a rotary evaporator. The yellow crystalline solid that precipitated was collected, washed with ether and dried in a vacuum to give the desired 5-methyl-pyridine-2-sulfonic acid [2-(3-hydroxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide as off-white crystals. ISP mass spectrum, m/e 495.2 (M+1 calculated for C24H22N4O6S1: 495). Melting point 211°-216° C.
後処理
- additionwas added
- temperatureThe solution was refluxed for 20 h
- customthe catalyst removed by filtration
- concentrationthe solution concentrated on a rotary evaporator
- customThe yellow crystalline solid that precipitated
- customwas collected
- washwashed with ether
- customdried in a vacuum
出典と根拠
- ORDレコード
- ord-d4d00f622d1a4fadaad775f5f73fa339
- 出典データセット
- uspto-grants-2001_06
- 特許番号
- US06242601B1
関連ノート
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