HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpyrrolidine → HCID 131716120, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpyrrolidine | HCID 8454 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 67833353 | HCID 67833353 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131716120 | HCID 131716120 | 88% |
Reaction Steps
To a solution of benzhydryl 7-tert-butoxycarbonylamino-3-iodomethyl-3-cephem-4-carboxylate-1-oxide (4.3 g) in dimethylformamide (70 ml) was added 1-methylpyrrolidine (0.63 g) at 0° C. The mixture was stirred for 1.5 hours under ice-cooling and poured into a mixture of ethyl acetate (700 ml) and ice-water (350 ml). The separated organic layer was washed with water, brine and dried over magnesium sulfate. The solvent was distilled off and the residue was pulverized in diisopropyl ether, collected by filtration and dried in vacuo to give powdery benzhydryl 7-tert-butoxycarbonylamino-3-(1-methyl-1-pyrrolidinio)methyl-3-cephem-4-carboxylate-1-oxide iodide (4.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04868174 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-61ed03712c064721bd64396ef7582e0f |
| Source note | uspto-grants-1989_09 |