反応 #56246

ord-f412a63e11db42a0a34eba6d101a1409

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONwas treated with 1.5 g of activated carbon
  2. 2
    ろ過was filtered
  3. 3
    洗浄The filter was washed twice with 5 ml of a 9-1 ethanol-water mixture
  4. 4
    workup.ADDITIONthe filtrate was added dropwise over 50 minutes
  5. 5
    workup.STIRRINGwith stirring at room temperature to 80 ml of ethanol which
  6. 6
    その他precipitation of the sodium salt
  7. 7
    workup.STIRRINGThe mixture was stirred for 2 hours at 0° C.
  8. 8
    ろ過filtered
  9. 9
    洗浄The crystals were washed with ethanol
  10. 10
    その他dried under reduced pressure

実験手順

10 g of the syn isomer of 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylic acid containing 7.2% of ethanol were added to a solution of 2 g of sodium acetate in 7.5 ml of water and 20 ml of absolute ethanol and the mixture was stirred for 15 minutes, was treated with 1.5 g of activated carbon and was filtered. The filter was washed twice with 5 ml of a 9-1 ethanol-water mixture and the filtrate was added dropwise over 50 minutes with stirring at room temperature to 80 ml of ethanol which caused precipitation of the sodium salt. The mixture was stirred for 2 hours at 0° C. and was vacuum filtered. The crystals were washed with ethanol and dried under reduced pressure to obtain 8.45 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 5.7% of water.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04224371uspto-grants-1980_09