HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 131718129, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-Boc-4-methylpiperazine | HCID 11401394 | — |
| Reactant | 7beta-[2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-carboxymethoxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylic acid | HCID 131718945 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131718129 | HCID 131718129 | 100.5% |
Reaction Steps
To a solution of 7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-carboxymethoxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylic acid (syn isomer) (4.0 g) in N,N-dimethylformamide was added dropwise 1-methyl-4-tert-butoxycarbonylpiperazine (6.7 g) at 2° C. under stirring. The stirring was continued for 1.5 hours at 18°-2° C. The reaction mixture was poured into ethyl acetate (200 ml). The resulting precipitates were collected by filtration to give 7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-carboxymethoxyiminoacetamido]-3-(1-methyl-4-tert-butoxycarbonyl-1-piperazinio)methyl-3-cephem-4-carboxylate hydrochloride (syn isomer) (5.71 g) .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05401734 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-294c00e467b54e739a68d0c524a76f1a |
| Source note | uspto-grants-1995_03 |