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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394103Generated: October 26, 2026

Ethyl 3-bromo-2-oxocyclohexanecarboxylate → Ethyl 2-amino-4,5,6,7-tetrahydrobenzthiazole-4-carboxyate hydrobromide

https://huagongshe.com/reaction/1394103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-bromo-2-oxocyclohexanecarboxylateHCID 121765—
ReactantThioureaHCID 2723790—
SolventEthanolHCID 702—
ProductEthyl 2-amino-4,5,6,7-tetrahydrobenzthiazole-4-carboxyate hydrobromideHCID 87730500—

Reaction Steps

Ethanol (50 mL) was added to ethyl 3-bromo-2-oxocyclohexane-carboxylate (50 g, 0.20 mol) and thiourea (15.3 g, 0.20 mol) and the reaction mixture was stirred for a period of 24 hours at room temperature under a blanket of nitrogen as inert gas. Following the removal of the solvent, ether (100 mL) was added to the residue. Following stirring for a period of 2 hours at room temperature, the suspension was filtered off and the solid matter was dried in vacuo. The product ethyl 2-amino-4,5,6,7-tetrahydrobenzthiazole-4-carboxyate hydrobromide was obtained in a yield of 58.6 g (corresponding to 95% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348347B2
Source datasetuspto-grants-2008_03
ORD IDord-9de07cbf27934ee28b6af45750699deb
Source noteuspto-grants-2008_03