Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 66692195 | HCID 66692195 | — |
| Product | HCID 66692138 | HCID 66692138 | — |
Reaction Steps
To a stirred solution of 5-(methyl-thio)-2-(pyridin-3-yl)-1H-benzo[d]imidazol-1-ol (0.36 g, 0.001 mol) in THF (20 ml) NaH (60% suspension in mineral oil), (0.14 g, 0.003 mol) was added. After stirring for the next 20 min at room temperature methyl iodide (0.39 g, 0.002 mol) was added drop wise. The resulting solution was continued to stir at room temperature for the next 3 h. The reaction was quenched with ice cold water and extracted with ethyl acetate (3×100 ml). The combined organic layers were washed with brine dried over Na2SO4 and concentrated under vacuum to afford to afford the crude compound which was purified by chromatography to obtain title compound 1-methoxy-5-(methyl-thio)-2-(pyridin-3-yl)-1H-benzo[ ]imidazole as a stick brown solid. 1H NMR (400 MHz, DMSO-d6), δ 9.47 (s, 1H), 8.74-8.73 (m, 1H), 8.53-8.50 (m, 1H), 7.71 (s, 1H), 7.49-7.33 (m, 3H), 4.05 (s, 3H) 2.58 (s, 3H). MS (M+1): 272.
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-16fd269d4f65487a9793df26fe47183b |
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| Source note | uspto-grants-2016_07 |
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