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HRID 445347Erstellt: 25. Oktober 2026

Dichloromethane → (R)-1-(4-(trifluoromethyl)phenyl)-N-((S)-1,1,1-trifluoropropan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxamide

https://huagongshe.com/reaction/445347

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
Edukt(S)-1,1,1-trifluoropropan-2-amineHCID 10964447—
Edukt(R)-1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinolineHCID 28293305—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(R)-1-(4-(trifluoromethyl)phenyl)-N-((S)-1,1,1-trifluoropropan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476297B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-59fb578bf90c4d3b95c357639152a83d
Quellennotizuspto-grants-2013_07