HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 7-Amino-3-[(5-carboxy-2-hydroxymethyl-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-3-cephem-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Reactant | HCID 178524652 | HCID 178524652 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Amino-3-[(5-carboxy-2-hydroxymethyl-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-3-cephem-4-carboxylic acid | HCID 131716546 | 65.8% |
Reaction Steps
In 130 ml of acetonitrile were suspended 8 g of 5-carboxy-2-hydroxymethyl-7-mercapto-s-triazolo[1,5-a]pyrimidine and 9.53 g of 7-aminocephalosporanic acid and 17 ml of boron trifluoride - ethyl ether complex was added thereto, and the mixture was stirred at room temperature for 5 hours. To the reaction mixture was added 300 ml of water and the mixture was adjusted to pH 2 with conc. aqueous ammonia. Precipitated crystals were collected by filtration, washed with water and with acetone, and dried to obtain 10.1 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04956462 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-ca76a69eb8644a89b9d7f5c9b92c97b1 |
| Source note | uspto-grants-1990_09 |