HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413439Generated: October 30, 2026
HCID 86739901, compound → HCID 86739900, compound
https://huagongshe.com/reaction/2413439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86739901 | HCID 86739901 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 86739900 | HCID 86739900 | 96.8% |
Reaction Steps
A solution of 2-benzhydryloxycarbonyl-3-[2-(2-t-butoxycarbonylamino-ethylthioacetamido)-thiazol-5-yl]-7-(3,4-dichlorophenylthio)-acetamido-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene (1.7 g) in formic acid (50 cc) is heated at 50° C. for 30 minutes and then concentrated to dryness under reduced pressure (2 mm Hg; 0.27 kPa) at 40° C. The oil which remains is taken up in acetone (20 cc), which is concentrated to dryness under reduced pressure (40 mm Hg; 5.3 kPa) at 50° C.; this operation is repeated once more and the residue is then taken up in boiling acetone (20 cc). The mixture is filtered hot and the solid collected is washed with acetone (20 cc) and ethyl ether (20 cc), to give 3-[2-(2-aminoethylthioacetamido)-thiazol-5-yl]-2-carboxy-7-(3,4-dichlorophenylthio)-acetamido-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene (1.15 g) in the form of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04496560 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-fe7bbdba2a9a492192566d34e6e3bf1c |
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| Source note | uspto-grants-1985_01 |
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