Trifluoromethanesulfonic acid 6-fluoroisoquinolin-3-yl ester → HCID 86633148, compound
Reaction equation
F[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[N:7][C:6]([O:12][S:13]([C:16]([F:19])([F:18])[F:17])(=[O:15])=[O:14])=[CH:5]2.O[C:21]1[N:22]=CC2C(C=1)=CC=CC=2C#N>>[C:21]([C:10]1[CH:11]=[CH:2][CH:3]=[C:4]2[C:9]=1[CH:8]=[N:7][C:6]([O:12][S:13]([C:16]([F:19])([F:18])[F:17])(=[O:15])=[O:14])=[CH:5]2)#[N:22]Participants
3
Procedure
Following the procedure for trifluoromethanesulfonic acid 6-fluoroisoquinolin-3-yl ester, using 3-hydroxyisoquinoline-8-carbonitrile in place of 6-fluoroisoquinolin-3-ol, the title compound was obtained as a yellow solid. MS (ES+): m/z=303.04 [MH+]. HPLC: tR=3.55 min (ZQ2, polar—5 min).
Sources & evidence
- ORD record
- ord-a2b3f5b44fde4e71b2dcbb01a91a3564
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08178668B2
Reaction notes
Loading…