Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 67980273 | HCID 67980273 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 67980256 | HCID 67980256 | — |
Reaction Steps
A mixture of 10-chloro-7-(5-cyclohexyl-pentyl)-7H-indolo[2,3-c]-quinoline (65 mg) in toluene (3 ml) and CH3I (0.3 mL) was stirred in a sealed pressure tube at 110° C. for 24 hours. The reaction mixture was allowed to cool to room temperature, diluted with Et2O (15 ml) and the resulting precipitate was filtered and washed with Et2O (3×20 ml) to yield the pure angular product as an orange solid (50 mg). Mp 246-248° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288410B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-061a8af88e3441e3aab8a478c159ad5e |
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| Source note | uspto-grants-2012_10 |
|---|