Acetamide, N-(trimethylsilyl)- → Benzhydryl 7beta-[2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylate

温度

-30 °C

A mixture of 2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetic acid (syn isomer) (2.4 g) and diisopropylethylamine (1.29 g) in N,N-dimethylformamide (35 ml) was cooled to -30° C. and mesyl chloride (1.15 g) was added dropwise thereto. The mixture was stirred at -20° to -30° C. for 30 minutes to give an activated acid solution. On the other hand, a mixture of benzhydryl 7β-amino-3-chloromethyl-3-cephem-4-carboxylate (2.18 g) and N-trimethylsilylacetamide (5.25 g) in methylene chloride (20 ml) was stirred to be a clear solution for 30 minutes at room temperature and then cooled to -20° C. To this solution was added the activated acid solution obtained above in one portion. The mixture was stirred for 30 minutes at -15° to -10° C., poured into water and extracted with ethyl acetate. The extract was washed with water three times, dried over magnesium sulfate and evaporated under reduced pressure. The residue was triturated in diisopropyl ether to give benzhydryl 7β-[2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylate (syn isomer) (4.64 g).

1. customto give an activated acid solution
2. stirringwas stirred
3. customfor 30 minutes
4. customat room temperature
5. temperaturecooled to -20° C
6. additionTo this solution was added the activated acid solution
7. customobtained above in one portion
8. stirringThe mixture was stirred for 30 minutes at -15° to -10° C.
9. extractionextracted with ethyl acetate
10. washThe extract was washed with water three times
11. dry with materialdried over magnesium sulfate
12. customevaporated under reduced pressure
13. customThe residue was triturated in diisopropyl ether

ORDレコード

ord-e160a36cf75141fc99b4ce8acbc4dc0a

出典データセット

uspto-grants-1990_10

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US04960766