Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 32818-79-4 | HCID 9576782 | — |
| Reactant | 2-Methylhexahydroisoquinoline-6,8(2H,7H)-dione | HCID 12855933 | — |
| Reactant | HCID 12868345 | HCID 12868345 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 5249961 | HCID 5249961 | 29% |
Reaction Steps
1,2,3,4,4a,7-Hexahydro-6,8-dimethoxy-2-methylisoquinoline (0.56 g, 2.68 mmol) was heated to 90°-100° in 70% aqueous acetic acid (10 ml) to hydrolyze the bis(enolether) to the octahydro-2-methylisoquinolin-6,8-dione. To the hot solution was added zinc dust (0.6 g, 9.25 mmol) and 2-isonitroso-3-pentanone (0.7 g, 6.1 mmol). The mixture was refluxed for 3 hours, cooled and filtered to remove zinc and zinc acetate. The filtrate was concentrated to dryness on a rotary evaporator and the residue was dissolved in dichloromethane. To the solution was added ammonium hydroxide and the layers were separated. The organic layer was washed with brine and dried over anhydrous sodium sulfate and concentrated to give the crude product. Chromatography of the crude product on Alumina III afforded 3-ethyl-2,6-dimethyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinolin-4-one as a white solid (0.19 g, 29% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04442291 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-aca55829dabb410a91167dc6a9fce1cd |
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| Source note | uspto-grants-1984_04 |
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