Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86729994 | HCID 86729994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86729993 | HCID 86729993 | 31.4% |
Reaction Steps
5-bromo-N-(1-methyl-1H-tetrazol-5-yl)pyridine-2-amine (1 g, 3.9 mmol) was dissolved in 50 mL THF, potassium tert-butylate (0.88 g, 7.8 mmol) and iodomethane (1.1 g, 7.8 mmol) were added slowly. The reaction was heated to 70° C. and reacted for 12 h. After filtration and concentration, 330 mg of product was obtained by separation on a silica gel column (dichloromethane:methanol=100:1), at a yield of 31%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359344B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-45248626c7ad48e8898e669b364b6589 |
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| Source note | uspto-grants-2016_06 |
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