HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → 6-Bromo-4H-imidazo[4,5-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | 5-Bromopyridine-2,3-diamine | HCID 691156 | — |
| Product | 6-Bromo-4H-imidazo[4,5-b]pyridine | HCID 911578 | 95% |
Reaction Steps
A suspension of 2,3-diamino-5-bromopyridine (3.0 g, 16.00 mmol) in formic acid (30 mL) was heated to reflux for 3 hours. After cooling the reaction mixture to room temperature it was concentrated and the residue was taken into 50% ethyl acetate in toluene (100 mL) then concentrated and the process repeated once more to remove excess formic acid. The resulting solid was triturated with ethyl acetate and the solid residue collected by filtration to give 6-bromo-1H-imidazo[4,5-b]pyridine (3.7 g, 95%). GCMS (EI) for C6H4BrN3: 198 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08648066B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-7b5ae499fc8644f7b92cf2b1a9766e7a |
| Source note | uspto-grants-2014_02 |