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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178211Generated: November 1, 2026

Chlorosuccinimide → Ethyl 2-amino-5-chloro-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/2178211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantEthyl 2-aminothiazole-4-carboxylateHCID 73216—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-amino-5-chloro-1,3-thiazole-4-carboxylateHCID 2178030498.4%

Reaction Steps

Ethyl 2-aminothiazole-4-carboxylate (4.72 g, 27.4 mmol) was combined with N-chlorosuccinimide (4.0 g, 30 mmol) and dissolved in acetonitrile (50 mL). The mixture was heated at mild reflux (>81.5° C.) for 5 hours. Subsequently, the flask was cooled to rt and decolorizing carbon was added to the mixture which was further diluted with EtOAc. The resulting slurry was filtered through a pad of silica and concentrated under reduced pressure to provide 5.57 g (98%) of the desired product ethyl 2-amino-5-chlorothiazole-4-carboxylate (1H). The analytical data on this compound corresponded to that previously reported (see. South. M. S. J. Heterocyclic Chem. 1991, 28, 1003).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067928B2
Source datasetuspto-grants-2015_06
ORD IDord-2a18ecc7fb454e7d9df49ccbfaf4c093
Source noteuspto-grants-2015_06