반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][C:7]([NH:9][CH:10]1[C:31](=[O:32])[N:12]2[C:13]([C:18]([O:20]CC3C=CC([N+]([O-])=O)=CC=3)=[O:19])=[C:14](O)[CH2:15][S:16][C@H:11]12)=[O:8].ClC(F)C(N(CC)CC)(F)[F:36]>C(Cl)Cl>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][C:7]([NH:9][CH:10]1[C:31](=[O:32])[N:12]2[C:13]([C:18]([OH:20])=[O:19])=[C:14]([F:36])[CH2:15][S:16][C@H:11]12)=[O:8]참가 물질
4
실험 절차
To a solution of 325 mg. (0.7 mmole) of p-nitrobenzyl 7-[2-(2-thienyl)acetamido]-3-hydroxy-3-cephem-4-carboxylate in 10 ml. of methylene chloride was slowly added an equivalent amount of N-(2-chloro-1,1,2-trifluoroethyl) diethylamine. The reaction mixture was heated for 30 minutes under gentle reflux and was then evaporated to dryness in vacuo. The residue was dissolved in a mixture of ethyl acetate-water and the organic layer was separated. The organic layer was washed with 5% hydrochloric acid, water and brine and was then dried. The dried reaction product solution was concentrated to a small volume and n-hexane was added to precipitate, p-Nitrobenzyl 7-[2-(2-thienyl)acetamido]-3-fluoro-3-cephem-4-carboxylate.
후처리
- temperatureThe reaction mixture was heated for 30 minutes
- temperatureunder gentle reflux
- customwas then evaporated to dryness in vacuo
- dissolutionThe residue was dissolved in a mixture of ethyl acetate-water
- customthe organic layer was separated
- washThe organic layer was washed with 5% hydrochloric acid, water and brine
- customwas then dried
- customThe dried reaction product solution
- concentrationwas concentrated to a small volume and n-hexane
- additionwas added
- customto precipitate
출처 및 근거
- ORD 기록
- ord-5ccefeceb80b4ca88ef12398562d5de5
- 출처 데이터셋
- uspto-grants-1977_12
- 특허 번호
- US04064343
연결된 노트
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