Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 66693171 | HCID 66693171 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66692725 | HCID 66692725 | — |
Reaction Steps
To a solution of 5,6-difluoro-2-(5-fluoropyridin-3-yl)-1H-benzo[d]imidazol-1-ol 0.15 g, 0.0003 mol) in THF (3.5 ml) was added NaH (0.045 g, 0.0011 mol) at room temperature. After stirring for 5 min at room temperature MeI (0.04 mL, 0.00059 mol) was added in one shot and further stirred for another 1 hr. After the consumption of the starting material (by TLC) the reaction mixture was washed with H2O and extracted with EtOAc (2×30 mL). The organic phase was dried and concentrated under vacuum. The crude was washed with Hexanes and further purified by chromatography (5-40% EtOAc/Hexanes) to give the desired compound 372 as a white solid. 1H NMR (400 MHz, DMSO-d6), δ: 9.28 (s, 1H), 8.62 (s, 1H), 8.24 (s, 1H), 7.58 (s, 1H), 7.32 (s, 1H), 4.06 (s, 3H). MS (M+1): 280, Purity 99.67%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382226B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-aea9a952ec1e4a1fb607d513865f0c0e |
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| Source note | uspto-grants-2016_07 |
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