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Formate → Sodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylate

HRID 27969
ノート
印刷プレビュー

反応式

HRID 27969 の反応式
C([O-])=O.[C:4]([O:7][CH2:8][C:9]1[CH2:10][S:11][C@@H:12]2[CH:19]([NH:20][C:21](=[O:32])[C:22]([C:26]3[N:27]=[C:28]([NH2:31])[S:29][CH:30]=3)=[N:23][O:24][CH3:25])[C:18](=[O:33])[N:13]2[C:14]=1[C:15]([OH:17])=[O:16])(=[O:6])[CH3:5].C([O-])(=O)C.[Na+:38]>O.C(O)C>[C:4]([O:7][CH2:8][C:9]1[CH2:10][S:11][C@@H:12]2[CH:19]([NH:20][C:21](=[O:32])[C:22]([C:26]3[N:27]=[C:28]([NH2:31])[S:29][CH:30]=3)=[N:23][O:24][CH3:25])[C:18](=[O:33])[N:13]2[C:14]=1[C:15]([O-:17])=[O:16])(=[O:6])[CH3:5].[Na+:38]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 283FormateHCID 517045Sodium AcetateHCID 1317115033-Acetoxymethyl 7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylic acid

生成物 1

HCID 131711736Sodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylate収率 0.95%

試薬・触媒・溶媒 2

HCID 702Ethanol
溶媒
HCID 962Water溶媒

実験手順

10 g of the formate solvate of the syn isomer of 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylic acid (described in Belgium Pat. No. 850,662) were added at room temperature to a solution of 3.5 g of sodium acetate in 5 ml of water and 300 ml of ethanol and when dissolution was complete, the mixture was filtered. The filtrate was added dropwise over one hour with stirring at room temperature to 160 ml of absolute ethanol and the resulting mixture was stirred at room temperature for 3 hours and at 0° C. for 16 hours. The mixture was vacuum filtered and the crystals were washed with ethanol and dried under reduced pressure to obtain 7.75 g of the crystalline D form of the syn isomer of sodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylate containing 0.95% of water.

後処理

  1. filtrationthe mixture was filtered
  2. additionThe filtrate was added dropwise over one hour
  3. stirringthe resulting mixture was stirred at room temperature for 3 hours and at 0° C. for 16 hours
  4. filtrationfiltered
  5. washthe crystals were washed with ethanol
  6. customdried under reduced pressure

出典と根拠

ORDレコード
ord-39112f5f0b064c6794dc4d0d27cfd8e6
出典データセット
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04224371

反応ノート

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