HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704492Generated: October 30, 2026
Ammonia → 7-Amino-3-[(2-hydroxymethyl-5-methyl-s-triazolo[1,5-a]pyrimidin7-yl)thiomethyl]-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/704492
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 7-Aminocephalosporanic acid | HCID 441328 | — |
| Reactant | HCID 178429718 | HCID 178429718 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Amino-3-[(2-hydroxymethyl-5-methyl-s-triazolo[1,5-a]pyrimidin7-yl)thiomethyl]-3-cephem-4-carboxylic acid | HCID 131716540 | — |
Reaction Steps
In 130 ml of acetonitrile were suspended 11.08 g of 2-hydroxymethyl-7-mercapto-5-methyl-s-triazolo[1,5-a]pyrimidine and 15.38 g of 7-aminocephalosporanic acid, and 24.6 ml of boron trifluoride - ethyl ether complex was added thereto and the mixture was stirred at 50° C. for 2 hours. After the reaction mixture was ice-cooled, 300 ml of water was added thereto and pH thereof was adjusted to 2 with conc. aqueous ammonia. The precipitated crystals were collected by filtration, washed with water and with acetone, and then dried to obtain 18.5 of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04987129 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-82da9403291f47639c3c5217e64c4a51 |
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| Source note | uspto-grants-1991_01 |
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