HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → N-methylpyridine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22040962 | HCID 22040962 | — |
| Product | N-methylpyridine-2-carboxamide | HCID 12272691 | — |
Reaction Steps
To a solution of ((5-aminobenzimidazol-2-yl)(4-bromophenylamine (1 eq) in N,N-dimethylformamide was added sodium hydride (2 eq) and the mixture was microwaved for 8 mins at 220° C. The reaction mixture was partitioned between ethyl acetate and water and the organic layer was dried with sodium sulfate and concentrated. Preparative chromatography yielded [4-({2-[(4-bromophenyl)amino}benzimidazol-5-yl}amino)(2-pyridyl-N-methylcarboxamide. MS: MH+=437.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728010B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-c7a9d1d99c204588a1e625c78dd8232b |
| Source note | uspto-grants-2010_06 |