HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → Phenacyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Phenacyl bromide | HCID 6259 | — |
Reaction Steps
Synthesis of 2-amino-4-arylimidazolamine of the formula (48) (wherein R4, R5, R6, R7 R8 and R9 are as defined above) is described in Scheme 9. Thus, reaction of acetophenone derivative of formula (45) with bromine in acetic acid gives phenacyl bromide, which on reaction with acetyl guanidine in acetonitrile at reflux temperature gives N-acetyl imidazole of the formula (47). The N-deacetylation of (47) under acidic conditions affords 2-amino-4-arylimidazoles of the formula (48). This is similar to the procedure reported by Thomas, L. et al in J. Org. Chem., 1994, 59, 7299-7305.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987278B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-d4c12c3bc1bc40b880395d771cb47b98 |
| Source note | uspto-grants-2015_03 |