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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394104Generated: October 25, 2026

Triethylamine → Ethyl 2-(3,3-dimethylbutyrylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylate

https://huagongshe.com/reaction/1394104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,3-Dimethylbutanoyl chlorideHCID 81514—
ReactantEthyl 2-amino-4,5,6,7-tetrahydrobenzthiazole-4-carboxyate hydrobromideHCID 87730500—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-(3,3-dimethylbutyrylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylateHCID 59681875—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethyl 2-amino-4,5,6,7-tetrahydrobenzthiazole-4-carboxyate hydrobromide (0.92 g, 0.3 mol) in acetonitrile (25 mL) there was added triethylamine (Et3N, 0.41 g, 0.4 mol). Following cooling to 0° C., tert-butylacetyl chloride (0.55 g, 0.4 mol) was slowly added, and the resultant mixture was then stirred overnight at room temperature. Following removal of the solvent and purification by column chromatography, there was obtained ethyl 2-(3,3-dimethylbutyrylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylate in a yield of 185 mg (corresponding to 19% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348347B2
Source datasetuspto-grants-2008_03
ORD IDord-318e770d7ce649978a8738cfab6f72d1
Source noteuspto-grants-2008_03