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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363763Generated: October 29, 2026

Ethyl 2-(2-aminothiazol-5-ylthio)acetate → HCID 57668386, compound

https://huagongshe.com/reaction/1363763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(2-aminothiazol-5-ylthio)acetateHCID 21455623—
Reactant4-[(Cyclopentylmethyl)amino]benzene-1-sulfonamideHCID 43453776—
Reactant{2-[3-Cyclopentylmethyl-3-(4-methanesulfonyl-phenyl)-ureido]thiazol-4-yl}-acetic acidHCID 57668194—
ReactantHCID 86629896HCID 86629896—
ProductHCID 57668386HCID 57668386—

Reaction Steps

The title compound was prepared via {2-[3-cyclopentylmethyl-3-(4-sulfamoyl-phenyl)-ureido]-thiazol-5-ylsulfanyl}-acetic acid ethyl ester in a similar manner as described for the synthesis of {2-[3-cyclopentylmethyl-3-(4-methanesulfonyl-phenyl)-ureido]-thiazol-4-yl}-acetic acid, using cyclopentylmethyl-(4-sulfamoyl-phenyl)-amine and (2-amino-thiazol-5-ylsulfanyl)acetic acid ethyl ester

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884210B2
Source datasetuspto-grants-2011_02
ORD IDord-a3a0858a00384b0cbbdf7a7f7171087c
Source noteuspto-grants-2011_02