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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524414Generated: October 25, 2026

Thiourea → Ethyl 2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-6-carboxylate

https://huagongshe.com/reaction/524414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
ReactantEthyl 3-bromo-4-oxocyclohexane-1-carboxylateHCID 12917737—
SolventEthanolHCID 702—
ProductEthyl 2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-6-carboxylateHCID 1510110180%

Reaction Steps

Thiourea (0.672 g, 8.835 mmol) was taken in ethanol (30 mL). To this stirred solution was added 3-Bromo-4-oxo-cyclohexane carboxylic acid ethyl ester (2.2 g, 8.835 mmol). The reaction was refluxed for 2 hrs. The reaction mixture was allowed to cool to room temperature and ethanol was evaporated under reduced pressure, the residue was partitioned between water and ethyl acetate. The water layer was collected and basified using sat. sodium bicarbonate solution, extracted with ethyl acetate, the organic layer was washed with brine, dried over anhydrous sodium sulfate filtered and concentrated under reduced pressure to afford 2-Amino-4,5,6,7-tetrahydro-benzothiazole-6-carboxylic acid ethyl ester (1.6 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340506B2
Source datasetuspto-grants-2016_05
ORD IDord-8222c4bc41444d6ca27ce59fbd284668
Source noteuspto-grants-2016_05