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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638836Generated: October 31, 2026

Benzo(d)thiazol-2-amine → ethyl imidazo[2,1-b][1,3]benzothiazole-2-carboxylate

https://huagongshe.com/reaction/638836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(d)thiazol-2-amineHCID 8706—
ReactantEthyl bromopyruvateHCID 66144—
SolventDimethylformamideHCID 6228—
Productethyl imidazo[2,1-b][1,3]benzothiazole-2-carboxylateHCID 1480574—

Reaction Steps

Ethyl bromopyruvate (9.8 g, 50 mmol) was added dropwise to a stirred solution of 2-aminobenzothiazole (7.5 g, 50 mmol) in DMF (100 ml) at room temperature. After the addition, the reaction mixture was heated to reflux for 6 h. The reaction mixture was cooled to room temperature and quenched with ice cold water. The aqueous layer was neutralized with NH4OH and the separated solid was filtered. It was washed well with water and dried. The crude product obtained was taken to next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691842B2
Source datasetuspto-grants-2010_04
ORD IDord-826f3b8e42574ee88dab8d45fe1c9626
Source noteuspto-grants-2010_04