Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178511839 | HCID 178511839 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178502852 | HCID 178502852 | — |
Reaction Steps
The combined extracts (upper layer + extracted layer) were combined and by adding cold methanol, the total volume was brought to 200 ml. This methanolic solution containing cefatrizine was added slowly to methanol, kept at a constant pH 5.1 by automatic addition of 10% triethylamine in methanol. The mixture was further stirred for one hour and then kept overnight at about -15° C. The crystalline precipitate was filtered, washed with 95% methanol and 99% methanol, respectively and dried in vacuo to constant weight. The yield was 8.408 g. of 7-[D-α-amino-p-hydroxyphenylacetamido]-3-[(1H)-1,2,3-triazol-5-yl-thiomethyl]-3-cephem-4-carboxylic acid-methanolate. The PMR spectrum of the product indicated an exact 1:1 ratio between cefatrizine and methanol, while crude yield of cefatrizine methanolate was 63.83%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04358588 |
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| Source dataset | uspto-grants-1982_11 |
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| ORD ID | ord-00982cd811dc44c989814ca9c3b8b08c |
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| Source note | uspto-grants-1982_11 |
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