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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452864Generated: October 29, 2026

Hydrochloric Acid → HCID 44515369, compound

https://huagongshe.com/reaction/452864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
ReactantLithium HydroxideHCID 3939—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 44515072HCID 44515072—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44515369HCID 44515369—

Reaction Conditions

Temperature100 °C

Reaction Steps

The title compound of Example 4, 1′-biphenyl-4-yl-1-[(3-methylpyridin-2-yl)methyl]-2′-oxo-1′,2′-dihydrospiro[piperidine-4,3′-pyrrolo[2,3-b]pyridine]-5′-carbonitrile, (1 mmol) was combined with anhydrous ethanol (10 mL) and neat sulfuric acid (1 mL) was added drop wise to the solution over 2 minutes. The resulting mixture is heated in a sealed tube to 100° C., allowed to cool to room temperature and combined with ice water. The resulting mixture was extracted with methylene chloride, dried and concentrated. The crude oil is combined with THF (10 mL), water (5 mL) and lithium hydroxide (20 mmol) and heated to 50° C. for 5 h, acidified with 1 m HCl, concentrated and purified by preparative reverse phase HPLC (method C), which provided the title compound, isolated as a salt of trifluoroacetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492398B2
Source datasetuspto-grants-2013_07
ORD IDord-4e8d83727b564344b065fe9ccc2574bc
Source noteuspto-grants-2013_07