HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → (7-Bromoimidazo[1,2-A]pyridin-2-YL)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 7-Bromo-2-chloromethylimidazo[1,2-a]pyridine | HCID 44118312 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (7-Bromoimidazo[1,2-A]pyridin-2-YL)methanamine | HCID 72209893 | — |
Reaction Steps
To a stirred solution of 7-Bromo-2-chloromethyl-imidazo[1,2-a]pyridine (0.325 g, 1.326 mmol) in methanol (5 mL), NH3 gas is purged at 0° C. for 30 minutes. The reaction is allowed to stir at room temperature for 16 hours. The solvent is concentrated to afford the title compound (0.315 g). 1H-NMR (400 MHz, DMSO-d6) δ: 4.15 (s, 2H), 7.12-7.15 (dd J1=1.96 Hz, J2=7.24 Hz, 1H), 7.90 (s, 1H), 8.03 (s, 1H), 8.32 (bs, 2H), 8.61 (d, J=7.2 Hz, 1H). LC-MS (m/z): [M+H]=225.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428528B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-9fde02022379480d916c8b78eaa90ebd |
| Source note | uspto-grants-2016_08 |