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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394109Generated: October 27, 2026

Water → 2-(2-Cyclohexylacetylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylic acid

https://huagongshe.com/reaction/1394109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(2-cyclohexylacetylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylateHCID 59681856—
SolventMethanolHCID 887—
Product2-(2-Cyclohexylacetylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylic acidHCID 59681868—

Reaction Steps

Water (20 mL) and MeOH (80 mL) were added to ethyl 2-(2-cyclohexylacetylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylate (F) (4.9 g, 14 mmol) and NaOH (5.6 g, 0.14 mol), and the resultant mixture was stirred at RT under a blanket of nitrogen as inert gas until completion of the reaction. Following removal of MeOH, 2N hydrochloric acid solution in water (250 mL) and DCM (250 mL) was added. The phases were separated, and the aqueous phase was extracted a number of times with DCM. Following drying of the combined organic phases over Na2SO4 and filtration, there was obtained the product 2-(2-cyclohexylacetylamino)-4,5,6,7-tetrahydrobenzthiazol-4-carboxylic acid (G) in a yield of 3.9 g (corresponding to 87% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348347B2
Source datasetuspto-grants-2008_03
ORD IDord-7b64f1cff8c7496689aaf0856ca094e8
Source noteuspto-grants-2008_03