Dichloromethane → (6R)-8-Oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

Temperatur

-15 °C

On the other hand, a mixture of 7-amino-3-[(1-hexyl-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acid (5.89 g) and trimethylsilyl acetamide (16 g) is methylene chloride (150 ml) was warmed to make a clear solution. The solution was cooled to -15° C. and added all at once to the activated acid solution prepared above. The reaction mixture was stirred for 30 minutes at -15° to 0° C. and for additional 30 minutes at ambient temperature. The solvent was removed by distillation from the reaction mixture under reduced pressure to give a residue, to which ethyl acetate (150 ml) and water (100 ml) were added, and then the mixed solution was adjusted to pH 3 with an aqueous solution of sodium bicarbonate. The organic layer was separated out, washed two times with an aqueous solution of sodium chloride and dried over magnesium sulfate, and then evaporated to dryness to give a brownish oil. This oil was washed three times with diethyl ether (70 ml) and triturated with diisopropyl ether to give a powder of 7-[2-(6-formamidopyridin-2-yl)-2-hydroxyiminoacetamido]-3-(1-hexyl-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acid (syn isomer), mp 74°-84° C. (dec.).

1. temperaturewas warmed
2. additionadded all at once to the activated acid solution
3. customprepared above
4. customThe solvent was removed by distillation from the reaction mixture under reduced pressure
5. customto give a residue
6. customThe organic layer was separated out
7. washwashed two times with an aqueous solution of sodium chloride
8. dry with materialdried over magnesium sulfate
9. customevaporated to dryness
10. customto give a brownish oil
11. washThis oil was washed three times with diethyl ether (70 ml)
12. customtriturated with diisopropyl ether

ORD-Eintrag

ord-807d5c91c63e42dc93d9643deff4e46b

Quelldatensatz

uspto-grants-1983_07

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04395411