Reaktionsgleichung
C[O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[N:8][CH:7]=[C:6]2[CH2:13][CH2:14][CH2:15][C:16]([F:19])([F:18])[F:17].B(Br)(Br)Br.BrC1C=C2C(C=CN=C2)=CC=1O>>[OH:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[N:8][CH:7]=[C:6]2[CH2:13][CH2:14][CH2:15][C:16]([F:19])([F:17])[F:18]Komponenten
4
Versuchsvorschrift
1.02 g of 6-Methoxy-4-(4,4,4-trifluoro-butyl)-isoquinoline (87) were treated with boron tribromide as described for the synthesis of compound 1 to give 410 mg of the desired product 88. LCMS Method # 1, retention time 1.04 min, detected mass 256.00 [M+H]+
Quellen und Nachweise
- ORD-Eintrag
- ord-b3ee4ab09bab40819a0ef29c1f391716
- Quelldatensatz
- uspto-grants-2013_08
- Patentnummer
- US08501736B2
Verknüpfte Notizen
Wird geladen…