HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → N-(5-cyanamido-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | N-(5-amino-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide | HCID 86677450 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(5-cyanamido-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide | HCID 86677452 | — |
Reaction Steps
To N-(5-amino-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (67) (4.53 g, 15 mmol) in MeOH (100 mL) was added KOAc (4.41 g, 45 mmol) and the mixture was stirred at room temperature for 5 minutes then cooled to 0° C. before a solution of BrCN (1.62 g, 15 mmol) in MeOH (30 mL) was added dropwise. The resulting mixture was slowly warmed to room temperature and stirred overnight. The solvent was evaporated and to the residue was added water (150 mL). The mixture was stirred at room temperature for 1 hour, filtered and washed with water (2×20 mL), then air dried to give N-(5-cyanamido-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (68) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754071B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-88da2bd1aa744843aafbbffa16b1b2b5 |
| Source note | uspto-grants-2014_06 |