HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596788Generated: November 1, 2026
Phosphate → 7-Acetoacetamido-3(5-methyl-1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/596788
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7-Acetoacetamido-3-acetoxymethyl-3-cephem-4-carboxylic acid | HCID 88715150 | — |
| Reactant | HCID 178434161 | HCID 178434161 | — |
| Product | 7-Acetoacetamido-3(5-methyl-1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid | HCID 131710660 | — |
Reaction Steps
A mixture of 0.356 g. of 7-acetoacetamido-3-acetoxymethyl-3-cephem-4-carboxylic acid, 0.84 g. of sodium hydrogen carbonate, 0.246 g. of 5-methyl-1,3,4-thiadiazol-2-thiol and 20 ml. of a phosphate buffer of pH 6.4 is heated at 60° C for 7.5 hours. After cooling, it is washed with ethyl acetate, adjusted to pH 2 with 50 % phosphoric acid, saturated with sodium chloride and extracted with ethyl acetate. The ethyl acetate layer is dried over magnesium sulfate and concentrated under reduced pressure, followed by cooling with ice. The resultant crystals are recovered by suction-filtration, washed with hexane and dried. The described procedure gives 7-acetoacetamido-3-(5-methyl-1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid as crystals melting at 177°-180° C (decomp.). Yield 0.274 g. (64 %).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04012379 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-4502d26896f54d8e880428a73e1204c2 |
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| Source note | uspto-grants-1977_03 |
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