HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Bromo-2-(1-methyl-1H-tetrazol-5-yl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Bromo-2-(2H-tetrazol-5-yl)pyridine | HCID 23438683 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Bromo-2-(1-methyl-1H-tetrazol-5-yl)pyridine | HCID 23438567 | — |
| Product | 5-Bromo-2-(2-methyl-2H-tetrazol-5-yl)pyridine | HCID 23438653 | — |
Reaction Steps
10.5 g of 2-(tetrazol-5-yl)-5-bromopyridine prepared in the Preparation example 6 was dissolved in 100 ml of dimethylformamide. And then 6.5 g of sodiumhydroxide was added to the solution and 9.3 g of iodomethane was slowly added to the solution at the temperature of 0° C. The solution was stirred for 6 hours at room temperature, added with water, extracted with ethyl acetate. And then the organic layer was washed with brine, dehydrated, filtrated, concentrated in vacuo and purified by column chromatography to obtain 4 g of 2-(1-methyltetrazol-5-yl)-5-bromopyridine and 5 g of 2-(2-methyltetrazol-5-yl)-5-bromopyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09163043B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-90a8cdac34d84cf7a1e1d95ef04f57fa |
| Source note | uspto-grants-2015_10 |