HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370597Generated: November 2, 2026
HCID 13175155, compound → HCID 13175157, compound
https://huagongshe.com/reaction/370597
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 13175155 | HCID 13175155 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 13175157 | HCID 13175157 | 84.7% |
Reaction Steps
A solution of 3-(2-acetamidothiazol-5-yl)-2-benzhydryloxycarbonyl-8-oxo-7-(thien-2-yl-acetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene (0.85 g) in formic acid (20 cc) is stirred for 30 minutes at 50° C. and then concentrated to dryness under reduced pressure (10 mm Hg; 1.3 kPa) at 40° C. The residue is taken up in ethanol (50 cc), the mixture is stirred for 5 minutes at 50° C. and the solvent is then evaporated off to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. The residue is taken up in ethanol (100 cc); the mixture is stirred for 10 minutes at 50° C. and the solid is then filtered off and washed with ethanol (3×15 cc) and ethyl ether (3×10 cc). After drying, 3-(2-acetamidothiazol-5-yl)-2-carboxy-8-oxo-7-(thien-2-yl-acetamido)-5-thia-1-azabicyclo [4.2.0]oct-2-ene (0.53 g) is obtained in the form of a light yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04526962 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-e74ecd2fc4164429b358a412a7ae3f1d |
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| Source note | uspto-grants-1985_07 |
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