HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromobenzene → HCID 57672140, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Aminopyrazine | HCID 78747 | — |
| Reactant | Ethyl 1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate | HCID 57619607 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 57672140 | HCID 57672140 | 99.2% |
Reaction Steps
211 mg of ethyl 1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate and 95 mg of aminopyrazine were added to 6 ml of bromobenzene, and the mixture was stirred for 3 hours under the heat-refluxing condition. The reaction mixture was cooled to room temperature, and t-butyl methyl ether was added to the mixture. The resulting solid was collected by filtration, washed with t-butyl methyl ether, and dried to obtain 258 mg of N-(2-pyrazinyl)-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxamide (hereinafter, referred to as present compound 1) represented by the formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943614B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-2671e7ac9d4f4aa28ae62c801dfbb121 |
| Source note | uspto-grants-2011_05 |