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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744916Generated: October 31, 2026

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

https://huagongshe.com/reaction/1744916

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 fitered. 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 numberUS07018997B2
Source datasetuspto-grants-2006_03
ORD IDord-63045a7327d34c5ca9b00b633ef3bf54
Source noteuspto-grants-2006_03