Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane | HCID 59337591 | — |
| Reactant | HCID 86761315 | HCID 86761315 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15603142 | HCID 15603142 | — |
Reaction Steps
(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane (70 mg) and 4-{5-[(cyclopropylmethyl)thio]-4-methyl-4H-1,2,4-triazol-3-yl}butyl methanesulfonate (70 mg) were dissolved in dimethylformamide (0.6 ml). Sodium Iodide (12 mg) and potassium carbonate (35 mg) were added. Reaction was heated at 60° C. for 20 h. Dichloromethane and NaHCO3 saturated solution were added. Solvent was removed, under reduced pressure, from organic phase. Crude was purified by silica column to give the free base of the title compound (5.5 mg). To a solution of this compound in DCM (0.5 mL), HCl 1N in diethylether (0.012 mL) was added and the solvent removed under reduced pressure to give the title compound as a slightly hygroscopic solid. (6.7 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07947683B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-1e6181f3d51b4c7c88d52611e61a10df |
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| Source note | uspto-grants-2011_05 |
|---|