Reacción #55420

Ecuación de reacción

7β-amino-7α-methoxy-3-[1-(2-t-butoxycarbonylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid t-butyl ester

N,N-diethylaniline

→

7β-D-Mandelamido-7α-methoxy-3-[1-(2-carboxyethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid

Disolventes

methylene chloride

methylene chloride

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGstirred for an additional 30 minutes
2. 2
   LavadoThe solution is washed with 50 ml
3. 3
   Secadoof cold 5% aqueous sodium bicarbonate, dried
4. 4
   Otroevaporated to dryness
5. 5
   workup.DISSOLUTIONThe residue is dissolved in a mixture of 10 ml
6. 6
   workup.STIRRINGof m-dmethoxybenzene and stirred at ambient temperature for 2 hours
7. 7
   OtroThe excess trifluoroacetic acid is evaporated under vacuum
8. 8
   Otrothe residue is partitioned between 50 ml
9. 9
   OtroThe organic phase is separated
10. 10
    workup.STIRRINGThe aqueous phase is stirred at pH 9.3-9.5 for 30 minutes
11. 11
    Extracciónextracted with 50 ml
12. 12
    ExtracciónThe aqueous layer is extracted with three 50 ml
13. 13
    Secadoportions of ethyl acetate and the combined extracts are dried
14. 14
    Otroevaporated to a small volume
15. 15
    workup.ADDITIONPetroleum ether is added dropwise
16. 16
    Otroto precipitate the title compound which
17. 17
    Filtraciónis collected by filtration
18. 18
    Otrodried

Procedimiento

A solution of 1.06 g. (2 mmol.) of 7β-amino-7α-methoxy-3-[1-(2-t-butoxycarbonylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid t-butyl ester and 0.30 g. (2 mmol.) of N,N-diethylaniline in 100 ml. of dry methylene chloride is stirred at 0°-5° while 0.56 g. (2 mmol.) of D-O-dichloroacetylmandeloyl chloride in 10 ml. of methylene chloride is added dropwise over 10 minutes. The mixture is stirred in the cold for 30 minutes then warmed to room temperature and stirred for an additional 30 minutes. The solution is washed with 50 ml. of cold dilute hydrochloric acid and 50 ml. of cold 5% aqueous sodium bicarbonate, dried and evaporated to dryness. The residue is dissolved in a mixture of 10 ml. of trifluoroacetic acid and 2 ml. of m-dmethoxybenzene and stirred at ambient temperature for 2 hours. The excess trifluoroacetic acid is evaporated under vacuum and the residue is partitioned between 50 ml. of ether and 50 ml. of water and adjusted to pH 9.3-9.5 with 5% aqueous sodium carbonate. The organic phase is separated and discarded. The aqueous phase is stirred at pH 9.3-9.5 for 30 minutes, extracted with 50 ml. of ethyl acetate which is discarded, layered with fresh ethyl acetate and adjusted to pH 1.5 with dilute hydrochloric acid. The aqueous layer is extracted with three 50 ml. portions of ethyl acetate and the combined extracts are dried and evaporated to a small volume. Petroleum ether is added dropwise to precipitate the title compound which is collected by filtration and dried.

Fuente