HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → benzhydryl 7-amino-3-[(Z)-2-(3-pyridyl)vinylthio]-3-cephem-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,3-Bis(trimethylsilyl)urea | HCID 87562 | — |
| Reactant | Benzhydryl 7-amino-3-mesyloxy-3cephem-4-carboxylate | HCID 88528619 | — |
| Product | benzhydryl 7-amino-3-[(Z)-2-(3-pyridyl)vinylthio]-3-cephem-4-carboxylate | HCID 67948113 | — |
Reaction Steps
The mixture was stirred for 30 minutes. To the mixture was added a solution of benzhydryl 7-amino-3-mesyloxy-3-cephem-4-carboxylate (9.21 g) and bis-(trimethylsilyl)urea (12.26 g) in acetonitrile (276 ml) under ice-cooling. The reaction mixture was stirred for 10 minutes at the same temperature. The insoluble material was filtered off. The filtrate was concentrated in vacuo and the residue was dissolved in ethyl acetate. The ethyl acetate solution was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo to give benzhydryl 7-amino-3-[(Z)-2-(3-pyridyl)vinylthio]-3-cephem-4-carboxylate (6.17 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04871730 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-28f01401d39e466cb67a7457e858887a |
| Source note | uspto-grants-1989_10 |