HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 131716544, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Reactant | HCID 178494658 | HCID 178494658 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 131716544 | HCID 131716544 | 49.7% |
Reaction Steps
In 600 ml of acetonitrile were suspended 30.1 g of 7mercapto-2-methoxymethyl-5-methyl-s-triazolo[1,5-a]pyrimidine and 38.9 g of 7-aminocephalosporanic acid and 68.7 ml of boron trifluoride - ethyl ether complex was added thereto, and the mixture was stirred at room temperature for 6 hours. One liter of water was added to the reaction mixture and the mixture was adjusted to pH 2 with addition of a conc. aqueous ammonia. The precipitated crystals were collected by filtration, washed with water and with acetone, and then dried to obtain 30 g of the title compound. 1H NMR (CF3COOD) δ: 2.87 (s, 3H), 3.70 (s, 3H), 3.86 (s, 2H), 4.78 (ABq, 2H), 5.24 to 5.68 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04987129 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-46c56e7c54d94ef78297049d1620565f |
| Source note | uspto-grants-1991_01 |