Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 70604705 | HCID 70604705 | — |
| Reactant | HCID 178434161 | HCID 178434161 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Phosphate | HCID 1061 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 70604919 | HCID 70604919 | — |
Reaction Steps
7-[α-Methylsulfonyl(2-furyl)acetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid (366.4 mg), 128 mg of 2-mercapto-5-methyl-1,3,4-thiadiazole and 68 mg of sodium bicarbonate were dissolved in a 0.1N phosphate buffer (pH 6.4), and the solution was stirred at 60° C. for 8 hours. Then, 20 ml of water, and 50 ml of ethyl acetate were added for extraction. The aqueous layer was acidified with 1H hydrochloric acid to a pH of 2, and extracted with ethyl acetate three times. The organic layer was washed four times with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, and concentrated under reduced pressure to obtain the product in powder form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04137406 |
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| Source dataset | uspto-grants-1979_01 |
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| ORD ID | ord-69aa6c47891f4b32bff4e687561f6df2 |
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| Source note | uspto-grants-1979_01 |
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