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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411276Generated: October 30, 2026

Methyl chloroformate → (S)-methyl 5-bromo-1-((5-((2-ethoxy-2-oxoethyl)thio)thiazol-2-yl)carbamoyl)spiro[indoline-3,3'-pyrrolidine]-1'-carboxylate

https://huagongshe.com/reaction/1411276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
Reactant2-Amino-5-chlorothiazole hydrochlorideHCID 148743—
ReactantEthyl 2-(2-aminothiazol-5-ylthio)acetateHCID 21455623—
Reactant(S)-t-butyl 5-bromospiro[indoline-3,3'-pyrrolidine]-1'-carboxylateHCID 90449438—
Product(S)-methyl 5-bromo-1-((5-((2-ethoxy-2-oxoethyl)thio)thiazol-2-yl)carbamoyl)spiro[indoline-3,3'-pyrrolidine]-1'-carboxylateHCID 90449800—

Reaction Steps

The captioned compound was obtained in the form of a white solid by performing the same reactions and/or treatments as those in Examples 1, 2, and 3, with the exceptions that (S)-t-butyl 5-bromospiro[indoline-3,3′-pyrrolidine]-1′-carboxylate was used instead of t-butyl 5-bromospiro[indoline-3,3′-pyrrolidine]-1′-carboxylate, that the ethyl 2-((2-aminothiazol-5-yl)thio)acetate synthesized by a method described in the known methods (International Publication WO2005/066145 etc.) was used instead of 2-amino-5-chlorothiazole hydrochloride, and that methyl chloroformate was used instead of acetyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921576B2
Source datasetuspto-grants-2014_12
ORD IDord-5f7adab4b8fd470395af31b90b244f27
Source noteuspto-grants-2014_12