HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → N-(2-amino-3-carbamoylphenyl)-6-(oxazol-5-yl)nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 2,3-Diaminobenzamide | HCID 10487029 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(2-amino-3-carbamoylphenyl)-6-(oxazol-5-yl)nicotinamide | HCID 66759969 | — |
Reaction Steps
A solution of EXAMPLE 50A (60.0 mg, 0.316 mmol) in a mixture of pyridine (1.5 mL) and N,N-dimethylformamide (1.5 mL) was treated with 1,1′-carbonyldiimidazole (56.3 mg, 0.347 mmol) at 45° C. for 2 hours. After cooling, 2,3-diaminobenzamide (HCl salt) (70.7 mg, 0.316 mmol) was added and the mixture stirred at room temperature for 5 hours. After concentration, the residue was treated with 20% brine and ethyl acetate. The solid was filtered, washed with ethyl acetate and water, and dried under vacuum to provide the title compound. This material was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08067613B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-961c1625352044ec8da9c7c71bcbf905 |
| Source note | uspto-grants-2011_11 |