HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382989Generated: October 31, 2026
HCID 57863259, compound → HCID 57863250, compound
https://huagongshe.com/reaction/2382989
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57863259 | HCID 57863259 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57863250 | HCID 57863250 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263605B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-70a0ceecc69d45aaa765df37f2e65693 |
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| Source note | uspto-grants-2012_09 |
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