Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405337Generated: October 30, 2026

Maleic Acid → trans-tert-butyl 5a',6',7',8',9',9a'-hexahydro-5'H-spiro[piperidine-4,4'-pyrrolo[1,2-a]quinoxaline]-1-carboxylate

https://huagongshe.com/reaction/1405337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AcidHCID 444266—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Reactanttrans-2-(1H-pyrrol-1-yl)cyclohexanamine hydrogen chlorideHCID 68153487—
SolventEthanolHCID 702—
Producttrans-tert-butyl 5a',6',7',8',9',9a'-hexahydro-5'H-spiro[piperidine-4,4'-pyrrolo[1,2-a]quinoxaline]-1-carboxylateHCID 131732186—

Reaction Conditions

Temperature80 °C

Reaction Steps

trans-2-(1H-Pyrrol-1-yl)cyclohexanamine hydrogen chloride (989 mg, 4.93 mmol), tert-butyl 4-oxopiperidine-1-carboxylate (982 mg, 4.93 mmol), and maleic acid (56.2 mg, 0.493 mmol) were combined in ethanol (12 mL). The reaction mixture was heated at 80° C. for 4 hours. The reaction mixture was cooled to room temperature and the solvent was evaporated. The residue was dissolved in dichloromethane and was then purified on 80 g of silica gel utilizing a gradient of 0-10% methanol in dichloromethane to give trans-tert-butyl 5a′,6′,7′,8′,9′,9a′-hexahydro-5′H-spiro[piperidine-4,4′-pyrrolo[1,2-a]quinoxaline]-1-carboxylate. ESI-MS m/z calc. 345.2, found 346.2 (M+1)+; Retention time: 1.63 minutes (4 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916565B2
Source datasetuspto-grants-2014_12
ORD IDord-c3368757f2b146c9bdf88f2748720674
Source noteuspto-grants-2014_12