Cefpodoxime → cefpodoxime sodium
反応式
C(C(CCCC)C([O-])=O)C.[Na+:11].[CH3:12][O:13][CH2:14][C:15]1[CH2:36][S:35][C@@H:18]2[C@H:19]([NH:22][C:23](/[C:25](/[C:29]3[N:33]=[C:32]([NH2:34])[S:31][CH:30]=3)=[N:26]\[O:27][CH3:28])=[O:24])[C:20](=[O:21])[N:17]2[C:16]=1[C:37]([OH:39])=[O:38]>CN(C)C(=O)C.CO>[CH3:12][O:13][CH2:14][C:15]1[CH2:36][S:35][C@@H:18]2[C@H:19]([NH:22][C:23](/[C:25](/[C:29]3[N:33]=[C:32]([NH2:34])[S:31][CH:30]=3)=[N:26]\[O:27][CH3:28])=[O:24])[C:20](=[O:21])[N:17]2[C:16]=1[C:37]([O-:39])=[O:38].[Na+:11]参加物
5
実験手順
2.03 g of sodium 2-ethylhexanoate was dissolved in a mixture of 12.5 ml of N,N-dimethylacetamide and 50 ml of methanol, 5.0 g of cefpodoxime (7-[2-(2-amino-4-thiazolyl)-(Z)-2-(methoxyimino)acetamido]-3-methoxymethyl -3-cephem-4-carboxylic acid) was added thereto, and the mixture was stirred at room temperature for 30 minutes. Then, methanol was removed under a reduced pressure and 50 ml of acetone was added thereto. The solution was stirred for 30 minutes and filtered. The filtered solid was washed with 50 ml of acetone and then with 30 ml of isopropyl ether, and vacuum-dried at room temperature to give 4.98 g of pale yellow cefpodoxime sodium salt (yield: 95%).
後処理
- additionwas added
- customThen, methanol was removed under a reduced pressure and 50 ml of acetone
- additionwas added
- stirringThe solution was stirred for 30 minutes
- filtrationfiltered
- washThe filtered solid was washed with 50 ml of acetone
- dry with materialwith 30 ml of isopropyl ether, and vacuum-dried at room temperature
出典と根拠
- ORDレコード
- ord-f6003448ddb3495688256b19219723b7
- 出典データセット
- uspto-grants-2003_10
- 特許番号
- US06639068B1
反応ノート
読み込み中…