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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615108Generated: October 31, 2026

Hydrochloric Acid → HCID 20429034, compound

https://huagongshe.com/reaction/615108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-Thiopheneacetyl chlorideHCID 162362—
ReactantHCID 20429062HCID 20429062—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 20429034HCID 2042903467.2%

Reaction Conditions

Temperature-55 °C

Reaction Steps

To a suspension of p-toluenesulfonic acid salt of benzyl 7-amino-8-oxo-3-trifluoromethanesulfonyl-5-thia-1,3-diazabicyclo[4,2,0]octane-2-carboxylate (800 mg.) in methylene chloride (8 ml.) was added pyridine (146 μl). After stirring at -55° C. for 5 minutes, 2-(2-thienyl)acetyl chloride (290 mg.) was added thereto, and then the mixture was gradually allowed to warm to 0° C. over a period of 1.5 hours. This mixture was poured into chilled dilute hydrochloric acid and extracted with ethyl acetate (50 ml.). The extract was washed with water (×2), a dilute aqueous solution of sodium bicarbonate, water and an aqueous solution of sodium chloride, successively. Drying over magnesium sulfate and removal of the solvent left an amorphous solid (800 mg.), which was chromatographed on silica gel (10 g.) with a mixed solvent of methylene chloride and ethyl acetate (95:5 to 90:10 by volume) to give benzyl 7-[2-(2-thienyl)acetamido] -8-oxo-3-trifluoromethanesulfonyl-5-thia-1,3-diazabicyclo[4,2,0]octane-2-carboxylate (667 mg.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04497738
Source datasetuspto-grants-1985_02
ORD IDord-a9b59e39d9cc4d0496b465171eeffa29
Source noteuspto-grants-1985_02