Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206188Generated: November 2, 2026

Hydrochloric Acid → HCID 178513595, compound

https://huagongshe.com/reaction/2206188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(4-oxo-1-(4-oxocyclohexyl)-4,5-dihydro-1H-pyrazolo[4,3-c]pyridin-3-yl)thiophene-2-carboxamideHCID 137010742—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178513595HCID 17851359576.8%

Reaction Steps

To a solution of 4-(4-oxo-1-(4-oxocyclohexyl)-4,5-dihydro-1H-pyrazolo[4,3-c]pyridin-3-yl)thiophene-2-carboxamide (40.0 mg) obtained in Example 170 in THF was added sodium borohydride (8.49 mg) at 0° C., and the mixture was stirred overnight at room temperature under nitrogen atmosphere. To the reaction solution was added 1N hydrochloric acid at 0° C., and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogencarbonate solution and saturated brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol) to give a cis/trans mixture (30.9 mg) of the title compound. The obtained cis/trans mixture was purified by HPLC (column: L-column2 ODS (trade name) 20 mmID×150 mmL, 5 μm, manufactured by Daicel Chemical Industries, mobile phase: water/acetonitrile (containing 10 mM ammonium carbonate)) to give the title compound having a shorter retention time.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371320B2
Source datasetuspto-grants-2016_06
ORD IDord-9f727e933c714b5db29b696ae0c97556
Source noteuspto-grants-2016_06