Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 57941362 | HCID 57941362 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57941485 | HCID 57941485 | 9% |
| Product | HCID 69018701 | HCID 69018701 | 16% |
Reaction Steps
Iodoethane (14 μL, 0.18 mmol) was added to (4S,7R)-2-(2-chloro-phenyl)-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (Intermediate 10; 47 mg, 0.16 mmol) and potassium carbonate (43 mg, 0.31 mmol) in dimethylformamide (1 mL). The mixture was heated at 60 degrees for 4 h, and then stirred at room temperature over the weekend. The reaction mixture was diluted with ethyl acetate and washed with NaOH. The solvent was evaporated from the ethyl acetate layer and the residue was purified by flash chromatography, eluting with 0-70% ethyl acetate/hexanes, to give 2-(2-chloro-phenyl)-3-ethoxy-7,8,8-trimethyl-4,5,6,7-tetrahydro-2H-4,7-methano-indazole (12.3 mg, 16%) and (4S,7R)-2-(2-chloro-phenyl)-1-ethyl-7,8,8-trimethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one (4.4 mg, 9%). APCI-MS (M+H) 331.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622492B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-c57f712bcfe3441383c43008e880fdf5 |
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| Source note | uspto-grants-2009_11 |
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