HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromobenzene → HCID 57672127, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | 6-Amino-3-chloropyridazine | HCID 21643 | — |
| Reactant | HCID 57619613 | HCID 57619613 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 57672127 | HCID 57672127 | 86.4% |
Reaction Steps
168 mg of ethyl 5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate and 82 mg of 3-amino-6-chloropyridazine were added to 1.5 ml of bromobenzene, and the mixture was stirred for 4 hours under heat refluxing. The reaction mixture was cooled to room temperature, and n-hexane was added to the reaction mixture. The resulting solid was collected by filtration, washed with a mixture of t-butyl methyl ether and n-hexane, and dried to obtain 180 mg of N-(6-chloro-3-pyridazinyl)-5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxamide (hereafter, referred to as present compound 17) 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-2c24126f38af41008bd818188b126e93 |
| Source note | uspto-grants-2011_05 |