HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → HCID 57619640, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | HCID 57619613 | HCID 57619613 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 57619640 | HCID 57619640 | 75.7% |
Reaction Steps
160 mg of ethyl 5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate and 60 mg of 2-aminothiazole were added to 1.5 ml of bromobenzene, then, the mixture was stirred for 5 hours under heat refluxing condition. The reaction mixture was cooled to room temperature, then, hexane was added to this and the resultant mixture was allowed to stand still. The resulting solid was collected by filtration, and washed with a mixture of t-butyl methyl ether and n-hexane and dried to obtain 136 mg of 5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-N-(2-thiazolyl)-1,2-d ihydropyridine-3-carboxamide (hereinafter, referred to as present compound 30) represented by the formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935716B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-de68aa8a0b9340a9b6e7d40984a917de |
| Source note | uspto-grants-2011_05 |