Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86729996 | HCID 86729996 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86729997 | HCID 86729997 | 4% |
Reaction Steps
1-(methoxymethyl)-4-amino-1H-1,2,3-triazole (3.56 g, 27.784 mmol), 2,5-dibromopyridine (19.608 g, 82.773 mmol) and potassium tert-butylate (9.345 g, 83.252 mmol) were added into DMF (100 mL), heated to 70° C., and stirred for 72 hours. The reaction solution was poured into water, and extracted with ethyl acetate. The combined organic phase was washed with a saturated solution of sodium chloride, dried over anhydrous sodium sulfate, concentrated, and separated on a silica gel column chromatograph (ethyl acetate:petroleum ether=1:30) to obtain 0.318 g of 5-bromo-N-(1-(methoxymethyl)-1H-1,2,3-triazol-4-yl)pyridine-2-amine as a yellow solid, at a yield of 4%.
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-f689e80a683d46e2a72ded2196c840ec |
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| Source note | uspto-grants-2016_06 |
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