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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744989Generated: October 30, 2026

Methanesulfonic Acid → Ethyl 5,6,7,8-tetrahydropyrazolo[5,1-b][1,3]benzoxazole-2-carboxylate

https://huagongshe.com/reaction/1744989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactantethyl-5-[(2-oxocyclohexyl)oxy]-1H-pyrazole-3-carboxylateHCID 178469286—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
ProductEthyl 5,6,7,8-tetrahydropyrazolo[5,1-b][1,3]benzoxazole-2-carboxylateHCID 2222448359.5%

Reaction Steps

A mixture of ethyl-5-[(2-oxocyclohexyl)oxy]-1H-pyrazole-3-carboxylate (127.6 mg, 0.5 mmol) and methane sulfonic acid (95 mg) in 5 ml of acetic acid and toluene (50 ml) was refluxed for 18 hours using a Dean-Stark trap to remove water. The reaction mixture was allowed to cool to room temperature. The reaction mixture was filtered. The filtrate was concentrated to an oil. The residue was dissolved in ethyl acetate and aqueous bicarbonate solution. The organic layer was washed with water and dried over MgSO4. After removal of the ethyl acetate, the residue was purified by silica gel chromatography eluting with 1:1 ethyl acetate/hexane to give 69.7 mg (59%) of the desired product as white solid. Mp; 55–57° C.; Electrospray-MS m/z 235.0 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07018997B2
Source datasetuspto-grants-2006_03
ORD IDord-cae0fa80c6eb4be1b3d22c6bc7e805d8
Source noteuspto-grants-2006_03