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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413414Generated: November 2, 2026

Methanesulfonic Acid → HCID 20430453, compound

https://huagongshe.com/reaction/2413414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant2-Thiopheneacetyl chlorideHCID 162362—
ReactantHCID 20430406HCID 20430406—
SolventAcetonitrileHCID 6342—
ProductHCID 20430453HCID 20430453—

Reaction Steps

On treating 3-[2-(4-acetamido-phenyl)-thiazol-5-yl]-2-benzhydryloxycarbonyl-7-t-butoxycarbonylamino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene (3.4 g) with methanesulphonic acid (3.4 cc) in acetonitrile (15 cc), in accordance with the working method described in Example 15, crude 7-amino-3-[2-(4-acetamido-phenyl)-thiazol-5-yl]-2-benzhydryloxycarbonyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene (2.9 g) is obtained, and this is acylated with (thien-2-yl)-acetyl chloride (0.62 cc) in accordance with the working method described in Example 1. The crude product obtained is purified by crystallisation from acetonitrile (200 cc). 3-[2-(4-Acetamido-phenyl)-thiazol-5-yl]-2-benzhydryloxycarbonyl-8-oxo-7-[(thien-2-yl)-acetamido]-5-thia-1-azabicyclo[4.2.0]oct-2-ene (1.33 g) is obtained in the form of a beige crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04496560
Source datasetuspto-grants-1985_01
ORD IDord-aa17b4f4708640f0b64409feffb1439c
Source noteuspto-grants-1985_01