反应详情

Phosphorus pentachloride (2.5 g.) was added with stirring and ice-cooling to a suspension of 2-dichloroacetoxyimino-2-(1,2,5-thiadiazol-3-yl)acetic acid (syn isomer) (3.7 g.) in dry methylene chloride (100 ml.), and the mixture was stirred for 1 hour at ambient temperature. The resultant mixture was concentrated and benzene was added thereto and distilled off (twice repeated). The residue was dissolved in dry methylene chloride. The solution was dropwise added with stirring and ice-cooling to a solution of 7-amino-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (3.9 g.) and bis(trimethylsilyl)acetamide (12 ml.) in dry methylene chloride (200 ml.). The resultant mixture was stirred for 1 hour at the same temperature and for 1 hour at ambient temperature. Methylene chloride was distilled off and to the residue were added ethyl acetate and water. After an insoluble material was filtered off, the ethyl acetate layer in the filtrate was washed three times with water, with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. The solvent was distilled off to give a residue (4.5 g.). The residue containing 7-[2-dichloroacetoxyimino-2-(1,2,5-thiadiazol-3-yl)acetamido]-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) was dissolved in a mixture of water and acetone, and the solution was stirred for 2 hours at ambient temperature and extracted with ethyl acetate. The extract was washed with water and with a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. The solvent was distilled off and the residue was dissolved in ethyl acetate. The solution was chromatographed on silica gel (5 g.) and the eluate was concentrated. The residue was reprecipitated from a mixture of ethyl acetate and ether, and the precipitates were collected by filtration, washed with ether and dried (3 g.). The powder was dissolved in distillated acetone, and the solution was treated with activated charcoal (3 g.) in column and then concentrated. The residue was reprecipitated from a mixture of acetone and ether. The precipitates was collected by filtration, washed with ether and dried to give 7-[2-hydroxyimino-2-(1,2,5-thiadiazol-3-yl)acetamido]-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (2.5 g.), mp 155° to 160° C. (dec.).

1. stirringthe mixture was stirred for 1 hour at ambient temperature
2. concentrationThe resultant mixture was concentrated
3. additionbenzene was added
4. distillationdistilled off (twice repeated)
5. dissolutionThe residue was dissolved in dry methylene chloride
6. additionThe solution was dropwise added
7. stirringwith stirring
8. temperatureice-cooling to a solution of 7-amino-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (3.9 g.) and bis(trimethylsilyl)acetamide (12 ml.) in dry methylene chloride (200 ml.)
9. stirringThe resultant mixture was stirred for 1 hour at the same temperature and for 1 hour at ambient temperature
10. distillationMethylene chloride was distilled off and to the residue
11. additionwere added ethyl acetate and water
12. filtrationAfter an insoluble material was filtered off
13. washthe ethyl acetate layer in the filtrate was washed three times with water
14. dry with materialwith a saturated aqueous solution of sodium chloride and dried over magnesium sulfate
15. distillationThe solvent was distilled off
16. customto give a residue (4.5 g.)
17. stirringthe solution was stirred for 2 hours at ambient temperature
18. extractionextracted with ethyl acetate
19. washThe extract was washed with water and with a saturated aqueous solution of sodium chloride
20. dry with materialdried over magnesium sulfate
21. distillationThe solvent was distilled off
22. dissolutionthe residue was dissolved in ethyl acetate
23. customThe solution was chromatographed on silica gel (5 g.)
24. concentrationthe eluate was concentrated
25. customThe residue was reprecipitated from a mixture of ethyl acetate and ether
26. filtrationthe precipitates were collected by filtration
27. washwashed with ether
28. customdried (3 g.)
29. dissolutionThe powder was dissolved in distillated acetone
30. additionthe solution was treated with activated charcoal (3 g.) in column
31. concentrationconcentrated
32. customThe residue was reprecipitated from a mixture of acetone and ether
33. filtrationThe precipitates was collected by filtration
34. washwashed with ether
35. customdried