HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dichloromethane → (R)-1-(4-(trifluoromethyl)phenyl)-N-((S)-1,1,1-trifluoropropan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Edukt | (S)-1,1,1-trifluoropropan-2-amine | HCID 10964447 | — |
| Edukt | (R)-1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinoline | HCID 28293305 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (R)-1-(4-(trifluoromethyl)phenyl)-N-((S)-1,1,1-trifluoropropan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxamide | HCID 59536364 | — |
Reaktionsschritte
To a solution of (S)-1,1,1-trifluoropropan-2-amine (90.9 μl, 884 μmol) in 4:1 CH2Cl2:THF (5 mL) is added di(1H-imidazol-1-yl)methanone (215 mg, 1326 μmol) and the flask was sealed and stirred at room temperature for 1.5 h. (R)-1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinoline (307 mg, 1105 μmol) was added and the reaction stirred at 2 h. The reaction was directly purified by reverse phase HPLC to give (R)-1-(4-(trifluoromethyl)phenyl)-N—((S)-1,1,1-trifluoropropan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxamide as a white powder. MS (ESI pos. ion) m/z: 417 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08476297B2 |
| Quelldatensatz | uspto-grants-2013_07 |
| ORD ID | ord-59fb578bf90c4d3b95c357639152a83d |
| Quellennotiz | uspto-grants-2013_07 |