Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 53402988 | HCID 53402988 | — |
Reaction Steps
A mixture of 2,5-dibromopyridine (500 mg) and methylhydrazine (1 mL) was heated at 100° C. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate and washed with a saturated brine. The organic layer was dried over sodium sulfate and concentrated in vacuo. The resultant crude product was purified by column chromatography on silica gel (solvent; chloroform) and the eluted fraction was concentrated. The residue was dissolved in tert-butanol and lyophilized to give 5-bromo-2-(N-methylhydrazino)pyridine (460 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188097B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-061311aa82cb4213be3f7c1e29bf8470 |
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| Source note | uspto-grants-2012_05 |
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