HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → (2-Amino-5-bromopyridin-3-yl)(6-bromopyridin-2-yl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 57690673 | HCID 57690673 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (2-Amino-5-bromopyridin-3-yl)(6-bromopyridin-2-yl)methanone | HCID 57690616 | 57.2% |
Reaction Steps
To a suspension of (2-aminopyridin-3-yl)(6-bromopyridin-2-yl)methanone (5.76 g, 20.7 mmol) in acetonitrile (120 ml) was added N-bromosuccinimide (4.05 g, 22.77 mmol). The resulting mixture was stirred at room temperature for 1 hour before mixture was concentrated in vacuo to approximately 20 ml. The solid was then collected by filtration and washed with minimal acetonitrile and dried to leave title compound as a brown solid (4.23 g, 57%). 1H NMR (DMSO-d6) 7.93-7.89 (4H, m), 8.03-7.99 (1H, m), 8.22 (1H, d), 8.36 (1H, d). ES+ 357.99.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08741931B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-d037a62513874dbb9293e3f8ec62d348 |
| Source note | uspto-grants-2014_06 |