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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370597Generated: November 2, 2026

HCID 13175155, compound → HCID 13175157, compound

https://huagongshe.com/reaction/370597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13175155HCID 13175155—
SolventFormic AcidHCID 284—
ProductHCID 13175157HCID 1317515784.7%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04526962
Source datasetuspto-grants-1985_07
ORD IDord-e74ecd2fc4164429b358a412a7ae3f1d
Source noteuspto-grants-1985_07