HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → p-Nitrobenzyl 7-amino-3-methylenecepham-4-carboxylate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | p-Nitrobenzyl 7-Penoxyacetamido-3-methylenecepham-4-carboxylate | HCID 20837924 | — |
| Solvent | Isobutanol | HCID 6560 | — |
| Product | p-Nitrobenzyl 7-amino-3-methylenecepham-4-carboxylate hydrochloride | HCID 70560152 | 58% |
Reaction Steps
To a solution of 965 mg. (2 mmole) of p-nitrobenzyl 7-phenoxyacetamido-3-methylenecepham-4-carboxylate in 10 ml. of methylene chloride were added 175 mg of dry pyridine and 460 mg. of phosphorus pentachloride and the mixture was stirred at room temperature for 6 hours. One ml. of isobutanol was added to the mixture which was then stored at 0° C. overnight. The reaction product, p-nitrobenzyl 7-amino-3-methylenecepham-4-carboxylate hydrochloride, which formed as a crystalline precipitate was filtered to yield 430 mg. (58% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04260745 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-4bc3b713208b448eb8ece3343bbbb4eb |
| Source note | uspto-grants-1981_04 |