Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 13261986 | HCID 13261986 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 178502830 | HCID 178502830 | 73.9% |
Reaction Steps
2.60 g of 7β-[2-(2-tritylaminothiazol-4-yl)-(Z)-2-methoxyiminoacetamido]-3-[(1-formamido-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acid were dissolved in 10 ml of 80% formic acid, and the solution was stirred at room temperature for one hour. 40 ml of water were added to the reaction solution, and insoluble materials were removed by filtration. The filtrate was condensed at a temperature below 40° C. under reduced pressure. One ml of tetrahydrofuran and 2 ml of ether were added to the residue, and the resultant precipitates were collected by filtration. 0.72 g of 7β-[2-(2-aminothiazol-4-yl)-(Z)-2-methoxyiminoacetamido]-3-[(1-formamido-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acid formate thus obtained as pale yellow powder were suspended in 8 ml of ethanol, and the suspension was stirred at 50° C. for 30 minutes. After cooling, the precipitates were collected by filtration. 0.53 g of 7β -[2-(2-aminothiazol-4-yl)-(Z)-2-methoxyiminoacetamido]-3-[(1-formamido-1H-tetrazol-5-yl)thiomethyl]-3cephem-4-carboxylic acid was thereby obtained as pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04576938 |
|---|
| Source dataset | uspto-grants-1986_03 |
|---|
| ORD ID | ord-000bf08ecc1b4554a7be27dcc2f6dcde |
|---|
| Source note | uspto-grants-1986_03 |
|---|