HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 131713642, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 131713644 | HCID 131713644 | — |
| Product | HCID 131713642 | HCID 131713642 | — |
Reaction Steps
5 g of 3-[(1-methyl-1H-tetrazol-5-yl)-thiomethyl]-7β-[(2R)-2-(4-BOC-aminophenyl)-2-(2-imidazolidone-1-carboxamido)-acetamido]-3-cephem-4-carboxylic acid diphenylmethyl ester are stirred at room temperature for 21/2 hours with 2.3 g of p-toluenesulphonic acid monohydrate in 50 ml of acetonitrile. After adding 500 ml of ether, filtering the precipitate with suction, washing with 300 ml of ether and drying in vacuo, 3-[(1-methyl-1H-tetrazol-5-yl)-thiomethyl]-7β-[(2R)-2-(4-aminophenyl)-2-(2-imidazolidone-1-carboxamido)-acetamido]-3-cephem-4-carboxylic acid diphenylmethyl ester p-toluenesulphonate is obtained [α]D20 =-37°±1° (0.758% in CH3OH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04464366 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-5b43ae5db19d4af28f464b26a569882f |
| Source note | uspto-grants-1984_08 |