HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Pivaloyloxymethyl 7-[(4-(3-aminopropyl)-1-piperidyl)-methyleneamino]-3-methyl-3-cephem-4-carboxylate, dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Pivaloyloxymethyl 7-[(4-(3-azidopropyl)-1-piperidyl)-methyleneamino]-3-methyl-3-cephem-4-carboxylate | HCID 131712136 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Pivaloyloxymethyl 7-[(4-(3-aminopropyl)-1-piperidyl)-methyleneamino]-3-methyl-3-cephem-4-carboxylate, dihydrochloride | HCID 131712137 | — |
Reaction Steps
To a stirred solution of pivaloyloxymethyl 7-[(4-(3-azidopropyl)-1-piperidyl)-methyleneamino]-3-methyl-3-cephem-4-carboxylate (1.5 g) in ethyl acetate (25 ml) were added water (30 ml) and hydrochloric acid to pH=3. 10% palladium-on-carbon (0.5 g) was added, and hydrogen was bubbled through the stirred mixture, a pH-value of 3 being maintained by addition of 0.2 N hydrochloric acid. When the consumption of acid ceased, the catalyst was filtered off. The aqueous phase was separated and freeze-dried to yield the desired compound as an amorphous powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04259333 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-6aaf4f2dad0b4a2ba35360a3f0956e89 |
| Source note | uspto-grants-1981_03 |