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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638907Generated: October 31, 2026

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

https://huagongshe.com/reaction/638907

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 numberUS07691842B2
Source datasetuspto-grants-2010_04
ORD IDord-b5120e7fe2694d9b839d960ad2aaa08a
Source noteuspto-grants-2010_04