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Phosphorus oxychloride → 2-Methyl-7-[2-methoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-cephem-4-carboxylic acid

HRID 28289
ノート
印刷プレビュー

反応式

HRID 28289 の反応式
[CH3:1][O:2][N:3]=[C:4]([C:8]1[N:9]=[C:10]([NH2:13])[S:11][CH:12]=1)[C:5]([OH:7])=O.P(Cl)(Cl)(Cl)=O.C[Si](CC(N)=O)(C)C.[CH3:27][CH:28]1[CH:33]=[C:32]([C:34]([OH:36])=[O:35])[N:31]2[C:37](=[O:40])[CH:38]([NH2:39])[C@H:30]2[S:29]1.C(=O)(O)[O-].[Na+]>C(OCC)(=O)C.CC(C)=O.O.CN(C)C=O>[CH3:27][CH:28]1[CH:33]=[C:32]([C:34]([OH:36])=[O:35])[N:31]2[C:37](=[O:40])[CH:38]([NH:39][C:5](=[O:7])[C:4](=[N:3][O:2][CH3:1])[C:8]3[N:9]=[C:10]([NH2:13])[S:11][CH:12]=3)[C@H:30]2[S:29]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

11

反応物 6

HCID 24813Phosphorus oxychloride2 回HCID 1252162-(2-Aminothiazole-4-yl)-2-methoxyiminoacetic acidHCID 357676Acetamide, 2-(trimethylsilyl)-HCID 516892Sodium Bicarbonate2 回HCID 128022512-Methyl-7-amino-3-cephem-4-carboxylic acidHCID 178502842HCID 178502842、化合物

生成物 1

HCID 1317114962-Methyl-7-[2-methoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-cephem-4-carboxylic acid

試薬・触媒・溶媒 4

HCID 180Acetone溶媒HCID 962Water溶媒HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒2 回

反応条件

温度
5 °C

実験手順

A suspension of 2-methoxyimino-2-(2-aminothiazol-4-yl)acetic acid (syn isomer), which can be represented as 2-methoxyimino-2-(2-imino-2,3-dihydrothiazol-4-yl)acetic acid (syn isomer), (26 g.) in ethyl acetate (250 ml.) was cooled to 5° C., and phosphorus oxychloride (25 g.) was added dropwise thereto with stirring under ice-cooling, and then the mixture was stirred for 30 minutes at 4° to 6° C. To the mixture was added dropwise a solution of trimethylsilylacetamide (22 g.) in ethyl acetate (20 ml.) with stirring under ice-cooling, and the mixture was stirred for 30 minutes at 4° to 6° C., and then phosphorus oxychloride (25 g.) was further added thereto with stirring under ice-cooling. The mixture was stirred for 15 minutes at the same temperature and dimethylformamide (10.6 g.) was added dropwise thereto at the same temperature. The mixture was stirred for 40 minutes at the same temperature, and the resulting clear solution was cooled to -10° C. On the other hand, to a solution of 2-methyl-7-amino-3-cephem-4-carboxylic acid (23.9 g.) in a solution of sodium bicarbonate (25 g.) and water (400 ml.) was added acetone (300 ml.), and the mixture was cooled to -5° C. To the mixture was added dropwise the above prepared clear solution at -5° to 0° C., and then the mixture was stirred for 2 hours, all the while the mixture was kept to pH 6 with 15% aqueous sodium bicarbonate solution. Insoluble materials were filterred off, and the aqueous layer was separated. The aqueous layer was adjusted to pH 3 with 20% hydrochloric acid, and precipitated crystals were collected by filtration, washed with water and acetone in turn and then dried under reduced pressure to give 2-methyl-7-[2-methoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-cephem-4-carboxylic acid (syn isomer), which can be represented as 2-methyl-7 -[2-methoxyimino-2-(2-imino-2,3-dihydrothiazol-4-yl)acetamido]-3-cephem-4-carboxylic acid (syn isomer), (39.4 g.). This object compound was identified with the object compound prepared in Example 6 by IR and NMR determination.

後処理

  1. temperaturecooling
  2. stirringthe mixture was stirred for 30 minutes at 4° to 6° C
  3. stirringwith stirring under ice-
  4. temperaturecooling
  5. stirringthe mixture was stirred for 30 minutes at 4° to 6° C.
  6. stirringwith stirring under ice-
  7. temperaturecooling
  8. additionwas added dropwise
  9. stirringThe mixture was stirred for 40 minutes at the same temperature
  10. temperaturethe resulting clear solution was cooled to -10° C
  11. temperaturethe mixture was cooled to -5° C
  12. additionTo the mixture was added dropwise the above prepared clear solution at -5° to 0° C.
  13. stirringthe mixture was stirred for 2 hours
  14. customthe aqueous layer was separated
  15. customprecipitated crystals
  16. filtrationwere collected by filtration
  17. washwashed with water and acetone in turn
  18. customdried under reduced pressure

出典と根拠

ORDレコード
ord-25dde54909534094a19b454ea7f1b23c
出典データセット
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04225707

反応ノート

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