HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 131715872, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-(Isocyanatocarbonyl)-1,2-phenylene diacetate | HCID 13364122 | — |
| Reactant | HCID 131715874 | HCID 131715874 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131715872 | HCID 131715872 | 72% |
Reaction Steps
In 10 ml of methanol was dissolved 0.41 g (0.47 mmole) of 7-{2-[2-amino-1,3-thiazol-4-yl]-2-[3-((3,4-diacetoxybenzoyl)carbamoyl)carbazoyl]methoxyiminoacetamido}-3-[(1,3,4-thiadiazol-2-yl)thiomethyl]-3-cephem-4-carboxylic acid hydrochloride obtained in Example 49, and 0.3 ml of 25% aqueous ammonia was added thereto and the mixture was stirred at room temperature for one hour. To the resulting solution was added 0.22 g (0.84 mmole) of 3,4-diacetoxybenzoylisocyanate and the mixture was stirred at room temperature for 8 hours. To the resulting mixture was added 20 ml of ether and resulting precipitates were collected by filtration, washed with ether and then dried to obtain 0.26 g of the title compound. (Yield: 70.3%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808711 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-92555f71ccf441c0b683edcbf26dc82e |
| Source note | uspto-grants-1989_02 |