HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366824Generated: November 2, 2026
Methyl iodide → 5-Bromo-N-methylpyridin-2-amine
https://huagongshe.com/reaction/2366824
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Bromo-N-methylpyridin-2-amine | HCID 15645663 | 23.6% |
Reaction Steps
NaH (47.3 mg, 1.971 mmol) and 5-bromo-2-pyridinamine (310 mg, 1.792 mmol, available from Aldrich) were added to N,N-Dimethylformamide (DMF) (7 mL) and stirred in an ice bath for 30 mins. The reaction mixture was then allowed to warm to room temperature and methyl iodide (0.123 mL, 1.971 mmol) was added and the reaction mixture stirred for 24 hr. The reaction mixture was partitioned between DCM (20 mL) and water (20 mL) and the organic layer washed with more water (20 mL) before being dried through an hydrophobic frit and concentrated. The residue was dissolved in DCM and purified by SP4 on a 25+S silica cartridge using a gradient of 10%-40% EtOAc in cyclohexane. Appropriate fractions were collected and concentrated to yield the desired product as a white solid (79.1 mg). LCMS (Method C): Rt 0.39, MH+=187
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08697725B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-62d4a30bb12f449587ab7aa55963bc3d |
|---|
| Source note | uspto-grants-2014_04 |
|---|