HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735781Generated: October 29, 2026
HCID 57847118, compound → HCID 57846922, compound
https://huagongshe.com/reaction/735781
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 57847118 | HCID 57847118 | — |
| Reactant | HCID 68576547 | HCID 68576547 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57846922 | HCID 57846922 | 17% |
Reaction Steps
A mixture of N-((1R,2S)-2-{[(3aR*,4R*,9bR*)-4-(3-thienyl)-2,3,3a, 4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinolin-1-yl]carbonyl}cyclohexyl)benzamide and N-((1R,2S)-2-{[(3aS*,4R*,9bS*)-4-(3-thienyl)-2,3,3a, 4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinolin-1-yl]carbonyl}cyclohexyl)benzamide (422 mg, 0.87 mmol) was dissolved in toluene (30 ml), manganese dioxide (7.6 g, 87 mmol) was added and the mixture was refluxed overnight. The reaction mixture was filtered through celite and washed with methanol. The filtrate was concentrated under reduced pressure. The residue was subjected to column chromatography using silica gel (30 g), and eluted with hexane-ethyl acetate (9:1-2:1, v/v). Crystallization from diisopropy ether gave the title compound (70 mg, 17%) as pale-brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592453B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-cb72ae8b2950490ba5342d26231b7aa9 |
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| Source note | uspto-grants-2009_09 |
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