HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-Bromo-6-(4-fluoro-phenyl)-imidazo[2,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Bromo-1-(4-fluorophenyl)ethan-1-one | HCID 96749 | — |
| Reactant | 5-Bromothiazol-2-amine monohydrobromide | HCID 2723848 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Bromo-6-(4-fluoro-phenyl)-imidazo[2,1-b]thiazole | HCID 24990705 | 20% |
Reaction Steps
To a solution of 2-bromo-1-(4-fluoro-phenyl)-ethanone (2 g, 9.215 mmol) in 100 ml ethanol were added 5-bromo-thiazol-2-ylamine hydrobromide (2.396 g, 9.215 mmol) and ethyl-diisopropyl-amine (1.19 g, 9.215 mmol). The mixture was stirred under reflux for 8 h and evaporated. Water was added to the residue and extracted with ethyl acetate. The organic layer was separated, washed with water, dried and evaporated. The crude product was purified by preparative HPLC (RP18, acetonitrile/water 0.1% TFA) to yield 532 mg (20%) of the desired product. MS: M+H+=296.96.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08080569B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-b9985385d8914badabdf7317b20ca8bc |
| Source note | uspto-grants-2011_12 |