HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromobenzene → HCID 66943785, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | HCID 67459179 | HCID 67459179 | — |
| Product | HCID 66943785 | HCID 66943785 | — |
Reaction Steps
In Scheme 6, Step A, a phenyl thiazolo-pyridinone of formula (22) is coupled with a phenyl bromide of formula (25a) or (25b) to give a thiazolo-pyridinone of formula (19) or formula (I). The reaction takes place in an inert solvent such as THF, or preferably dioxane with an inorganic base added, such as cesium carbonate. A copper catalyst is used, such as copper (I) iodide in the presence of sym-dimethylethylene diamine. The reaction is heated at a temperature of about 70° C. to the reflux temperature of the solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08049013B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-f63522cda6d94b4f93f637e03ee6c4da |
| Source note | uspto-grants-2011_11 |