Sodium Methoxide → HCID 11640716、化合物
反応式
[CH2:1]([O:3][C:4](=[O:35])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][C:12]2[CH:17]=[C:16]([NH:18][CH2:19][CH2:20][C:21]3[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[C:23]([O:29][CH3:30])[CH:22]=3)[N:15]=[C:14](S(C)(=O)=O)[N:13]=2)[CH:6]=1)C.[CH3:36][O-:37].[Na+]>COCCOC>[CH3:1][O:3][C:4](=[O:35])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][C:12]2[CH:17]=[C:16]([NH:18][CH2:19][CH2:20][C:21]3[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[C:23]([O:29][CH3:30])[CH:22]=3)[N:15]=[C:14]([O:37][CH3:36])[N:13]=2)[CH:6]=1参加物
4
実験手順
To a solution of above 3-{6-[2-(3,4-Dimethoxy-phenyl)-ethylamino]-2-methanesulfonyl-pyrimidin-4-yloxy}-benzoic acid ethyl ester [180 mg, 0.36 mmol, Intermediate (72)] in 1,2-dimethoxyethane (5 mL) is added a 25% solution of sodium methoxide (3 mL). After 1 h at 20° C., the mixture is filtered through a plug of SiO2 (EtOAc). The filtrate is concentrated to give 3-{6-[2-(3,4-dimethoxy-phenyl)-ethylamino]-2-methoxy-pyrimidin-4-yloxy}-benzoic acid methyl ester [70 mg, 44%, Example (63)]. LCMS: RT=3.34 minutes, MS: 440 (M+H). IC50=6254 nM
後処理
- filtrationthe mixture is filtered through a plug of SiO2 (EtOAc)
- concentrationThe filtrate is concentrated
出典と根拠
- ORDレコード
- ord-eaecbf56d8b648fba9014086f21fd1d6
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08193183B2
反応ノート
読み込み中…