HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-fluorophenyl)-1-(1,1,1-trifluoroprop-2-en-2-yl)phthalazin-6-amine → N-(4-Fluorophenyl)-1-(2,2,2-trifluoro-1-methylethyl)-6-phthalazinamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-fluorophenyl)-1-(1,1,1-trifluoroprop-2-en-2-yl)phthalazin-6-amine | HCID 66740077 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | N-(4-Fluorophenyl)-1-(2,2,2-trifluoro-1-methylethyl)-6-phthalazinamine | HCID 45280246 | — |
Reaction Steps
A solution of N-(4-fluorophenyl)-1-(1,1,1-trifluoroprop-2-en-2-yl)phthalazin-6-amine (0.067 g, 0.20 mmol) in 4 mL of THF/EtOH (3/1) was treated with palladium (10% wt. on activated carbon, 0.021 g, 0.020 mmol); and stirred at RT with a balloon of hydrogen. After 3 h, the reaction mixture was filtered through a pad of Celite and the filtrate was concentrated to give the crude product. The material was purified on an ISCO column (12 g, 50-75% EtOAc in hexanes) to afford the title compound as a light yellow solid. MS (ESI, pos. ion) m/z: M+1=366.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08497269B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-3530fa45ef50491a87db87ffb8178493 |
| Source note | uspto-grants-2013_07 |