Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | 6-Bromoindole | HCID 676493 | — |
| Reactant | Octahydroindolizin-7-one | HCID 11240524 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10083756 | HCID 10083756 | 169% |
Reaction Steps
To a suspension of potassium hydride (KH; 0.289 g, 7.2 mmol) in tetrahydrofuran (THF; 5 ml) at −10° C. was added, dropwise, a solution of 6-bromoindole (1.2 g, 6 mmol) in THF (1 ml). The mixture was stirred at this temperature for 20 mins, until no more evolution of hydrogen was observed. The mixture was then cooled to −78° C. in an acetone/dry ice bath, 8.82 ml of a 1.7M solution of tBuLi was added slowly, and the mixture stirred for another 30 mins. Azabicyclo[4,3,0]nonan-4-one (1.67 g. 1.2 mmol) was then added, and the mixture stirred at −78° C. for a further 30 mins before being quenched with a mixture of dichloromethane (50 ml) and pH7 buffer (50 ml). After filtration, the organic layer was washed with water and brine, dried, concentrated, and the residue triturated with hexanes to give 0.52 g of the title product as a white powder (33.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06716837B1 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-6555498af91f4639901d83821a110497 |
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| Source note | uspto-grants-2004_04 |
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