反応式
[CH3:1][S:2]([C:5]1[CH:36]=[CH:35][C:8]([CH2:9][NH:10][C:11]([C:13]2[C:14](=[O:34])[N:15]([C:24]3[CH:29]=[CH:28][CH:27]=[C:26]([C:30]([F:33])([F:32])[F:31])[CH:25]=3)[C:16]([CH3:23])=[C:17]([C:19](=O)[CH2:20]Br)[CH:18]=2)=[O:12])=[CH:7][CH:6]=1)(=[O:4])=[O:3].[NH2:37][C:38]([NH2:40])=[S:39].CC([O-])=O.[Na+]>CCO>[CH3:1][S:2]([C:5]1[CH:6]=[CH:7][C:8]([CH2:9][NH:10][C:11]([C:13]2[C:14](=[O:34])[N:15]([C:24]3[CH:29]=[CH:28][CH:27]=[C:26]([C:30]([F:33])([F:31])[F:32])[CH:25]=3)[C:16]([CH3:23])=[C:17]([C:19]3[N:37]=[C:38]([NH2:40])[S:39][CH:20]=3)[CH:18]=2)=[O:12])=[CH:35][CH:36]=1)(=[O:3])=[O:4]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 90 °C
実験手順
5-Bromoacetyl-6-methyl-2-oxo-1-(3-trifluoromethyl-phenyl)-1,2-dihydro-pyridine-3-carboxylic acid 4-methanesulfonyl-benzylamide (Example 50 (c), 0.04 g, 0.067 mmol), thiourea (0.0067 g, 0.086 mmol), NaOAc (0.011 g, 0.136 mmol), EtOH (2 ml) and a magnetic stirrer bar were placed in a tube designed for microwave synthesis. The vial was sealed and the mixture was heated in a CEM Discover Microwave apparatus (100 W, 90° C.) for 20 minutes, giving complete conversion of the starting material to a single product according to LC-MS. The solvents were evaporated to give a crude mixture which was purified on preparative HPLC giving the title compound (0.026 g, 66%) as a slightly yellowish solid after freeze-drying the pure fractions.
後処理
- customdesigned for microwave synthesis
- customThe vial was sealed
- customgiving complete conversion of the starting material to a single product
- customThe solvents were evaporated
- customto give a crude mixture which
- customwas purified on preparative HPLC
出典と根拠
- ORDレコード
- ord-1b3fe496dde14a2dab76905d463a6b62
- 出典データセット
- uspto-grants-2013_08
- 特許番号
- US08501784B2
関連ノート
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