HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lawesson's reagent → 5-Bromo-2-chloro-1-(2-phenyl-5-thiazolylmethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | 1-(3-Benzoylamino-2-oxopropyl)-5-bromo-2-chlorobenzene | HCID 66607452 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Bromo-2-chloro-1-(2-phenyl-5-thiazolylmethyl)benzene | HCID 66608645 | 72.5% |
Reaction Steps
To a solution of the above 1-(3-benzoylamino-2-oxopropyl)-5-bromo-2-chlorobenzene (710 mg) in toluene (20 ml) was added Lawesson reagent (2.35 g), and the mixture was heated under reflux for 2 hours. The reaction mixture was cooled, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=90:10) to give the desired 5-bromo-2-chloro-1-(2-phenyl-5-thiazolylmethyl)benzene (512 mg) as a colorless solid. APCI-Mass m/Z 364/366 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08785403B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-680c580525ab40d3a166e226c155ed71 |
| Source note | uspto-grants-2014_07 |