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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | trans-2-(1H-pyrrol-1-yl)cyclohexanamine hydrogen chloride | HCID 68153487 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | trans-tert-butyl 5a',6',7',8',9',9a'-hexahydro-5'H-spiro[piperidine-4,4'-pyrrolo[1,2-a]quinoxaline]-1-carboxylate | HCID 131732186 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916565B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-c3368757f2b146c9bdf88f2748720674 |
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| Source note | uspto-grants-2014_12 |
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