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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589839Generated: October 30, 2026

3-Quinuclidinol, (-)- → HCID 54088674, compound

https://huagongshe.com/reaction/1589839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Quinuclidinol, (-)-HCID 91404—
ReactantSodiumHCID 5360545—
ReactantEthyl 7-methylpyrazolo[1,5-a]pyridine-3-carboxylateHCID 19770966—
SolventBenzeneHCID 241—
ProductHCID 54088674HCID 5408867410.2%

Reaction Steps

After a suspension of 90 mg (0.71 mmol) of (R)-(-)-3-quinuclidinol, which had been prepared in accordance with the procedure disclosed in "Eur. J. Med. Chem.", 14, 111-114 (1979), in 15 ml of benzene was refluxed for 1.5 hours by using a Dean-Stark apparatus, 0.05 g of metal sodium was added and the resultant mixture was refluxed under stirring for further 2.5 hours. Unreacted sodium was removed and 100 mg (0.49 mmol) of ethyl 7-methylpyrazolo[1,5-a]pyridine-3-carboxylate were added, followed by heating under reflux for 24 hours. The solvent of the reaction mixture was distilled off under reduced pressure and the residue was purified by chromatography on a silica gel column (chloroform:methanol=10:1), whereby 15 mg (0.05 mmol) of the title compound were obtained as white crystals (yield: 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05200415
Source datasetuspto-grants-1993_04
ORD IDord-8e6ffd763ea74427baf7a9797d60c7c1
Source noteuspto-grants-1993_04