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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638848Generated: October 31, 2026

2-Amino-6-methylbenzothiazole → Ethyl 7-methylimidazo[2,1-b][1,3]benzothiazole-2-carboxylate

https://huagongshe.com/reaction/638848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-6-methylbenzothiazoleHCID 17335—
ReactantEthyl bromopyruvateHCID 66144—
ProductEthyl 7-methylimidazo[2,1-b][1,3]benzothiazole-2-carboxylateHCID 63859757.6%

Reaction Steps

Ethyl 7-methylimidazo[2,1-b]-benzthiazole-2-carboxylate was prepared according to the procedure as outlined in Example 1, (Step 1). Starting from 6-methyl-2-amino benzothiazole (3.2 g, 20 mmol) and ethyl bromopyruvate (4.0 g, 20.4 mmol), 3.0 g (57% Yield) of ethyl 7-methylimidazo[2,1-b]-benzthiazole-2-carboxylate was isolated as brown solid. (M+H) 261.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691842B2
Source datasetuspto-grants-2010_04
ORD IDord-480bbe16d45349ddabb275fd9489b7e4
Source noteuspto-grants-2010_04