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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957942Generated: November 2, 2026

Propargyl alcohol → HCID 59232565, compound

https://huagongshe.com/reaction/1957942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 10413921HCID 10413921—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventPyrrolidineHCID 31268—
ProductHCID 59232565HCID 5923256574.3%

Reaction Steps

To a stirred solution of 5-(4-Bromo-phenyl)-1-(2,4-dichloro-phenyl)-4-methyl-1H-pyrazole-3-carboxylic acid piperidin-1-ylamide (40 mg, 0.078 mmol) in pyrrolidine (2.5 ml) was added a catalytic amount of tetrakis(triphenylphosphine) palladium under an atmosphere of Argon. After stirring the contents for 5 min at room temperature, a solution of propargyl alcohol (10 mg, 0.178 m mol) in pyrrolidine (1.5 ml) was added to the reaction mixture. The contents were heated at 80-85° C. for 10 h. Then a saturated aqueous solution of ammonium chloride was added and the mixture was extracted with ethyl acetate. The organic extract was dried over MgSO4 and the solvent was removed in vacuo. Purification by flash column chromatography on silica gel (petroleum ether-ethyl acetate, 7:3) afforded 28 mg (74%) of 2-1 as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410097B2
Source datasetuspto-grants-2013_04
ORD IDord-8993e127bdd249258f57d5d330b17bf5
Source noteuspto-grants-2013_04