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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382989Generated: October 31, 2026

HCID 57863259, compound → HCID 57863250, compound

https://huagongshe.com/reaction/2382989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57863259HCID 57863259—
SolventEthanolHCID 702—
ProductHCID 57863250HCID 57863250—

Reaction Conditions

Temperature45 °C

Reaction Steps

The crude 1-benzyl-N,N-dimethyl-2′,3′-dihydro-1′H-spiro[piperidine-4,4′-quinoline]-1′-carboxamide 2ab (3.1 g, 8.01 mmol) was dissolved in 30 mL absolute ethanol, flushed with nitrogen, and treated with 500 mg of 10% Pd/C. The flask was flushed with nitrogen then fitted with an H2 balloon. The rapidly stirring solution was heated to 45° C. overnight. The reaction was filtered through Celite and concentrated to yield N,N-dimethyl-2′,3′-dihydro-1′H-spiro[piperidine-4,4′-quinoline]-1′-carboxamide 2ac as an amber oil. LC/MS (10-99% CH3CN/0.05% TFA gradient over 5 min): m/z 274.2, retention time 1.39 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263605B2
Source datasetuspto-grants-2012_09
ORD IDord-70a0ceecc69d45aaa765df37f2e65693
Source noteuspto-grants-2012_09