Sodium Hydroxide → HCID 44513409、化合物
反応式
[CH3:1][CH:2]([CH2:40][CH3:41])[CH:3]([C:20]1[CH:25]=[CH:24][C:23]([CH2:26][N:27]2[C:32](=[O:33])[CH2:31][O:30][C:29]([C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=3)=[N:28]2)=[CH:22][CH:21]=1)[C:4]([NH:6][C:7]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:8]=1[CH2:9][CH:10]([C:16]([O:18]C)=[O:17])[CH2:11]2)=[O:5].[OH-].[Na+]>C1COCC1>[CH3:1][CH:2]([CH2:40][CH3:41])[CH:3]([C:20]1[CH:25]=[CH:24][C:23]([CH2:26][N:27]2[C:32](=[O:33])[CH2:31][O:30][C:29]([C:34]3[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=3)=[N:28]2)=[CH:22][CH:21]=1)[C:4]([NH:6][C:7]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:8]=1[CH2:9][CH:10]([C:16]([OH:18])=[O:17])[CH2:11]2)=[O:5]参加物
4
実験手順
A solution of 180 mg (0.31 mmol) of methyl 4-[(3-methyl-2-{4-[(5-oxo-2-phenyl-5,6-dihydro-4H-1,3,4-oxadiazin-4-yl)methyl]phenyl}pentanoyl)amino]-2,3-dihydro-1H-indene-2-carboxylate (Example 147A) in 3.6 ml of THF and 1.3 ml (1.3 mmol) of 1 N aqueous sodium hydroxide solution was stirred at room temperature overnight. After the reaction had gone to completion, the THF was removed under reduced pressure and the reaction solution was diluted with water and then adjusted to pH 2 with 1 M hydrochloric acid. The precipitated solid was filtered off, washed with water and dried under reduced pressure at 45° C. overnight. This gave 159 mg (0.29 mmol, 91% of theory) of the title compound as a mixture of isomers.
後処理
- customthe THF was removed under reduced pressure
- additionthe reaction solution was diluted with water
- filtrationThe precipitated solid was filtered off
- washwashed with water
- customdried under reduced pressure at 45° C. overnight
- additionThis gave 159 mg (0.29 mmol, 91% of theory) of the title compound as a mixture of isomers
出典と根拠
- ORDレコード
- ord-506cd3df9af64af2991b691e4d02a149
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08987256B2
反応ノート
読み込み中…