Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | HCID 71110611 | HCID 71110611 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 71110548 | HCID 71110548 | 30.3% |
Reaction Steps
To a solution of compound 137 (200 mg, 0.35 mmol) and thiourea (53 mg, 0.70 mmol) in 1,4-dioxane (5.0 mL) was added TMSOTf (96 μL, 0.53 mmol) and the reaction mixture was heated to 80° C. for 3 h. The mixture was cooled to room temperature, and MeI (55 μL, 0.87 mmol) and DIPEA (0.30 mL, 1.75 mmol) were added thereto and the mixture was stirred for 3 h. The resulting mixture was diluted with EtOAc and washed with water. The organic layer was dried over dried over MgSO4, filtered, and concentrated in vacuo. The crude was purified by preparative HPLC (reverse phase) to provide the title compound (60 mg, 30%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034921B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-b40e8b56026747238e0868ea00db811f |
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| Source note | uspto-grants-2015_05 |
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