2-Quinolinecarbonitrile,6-amino-(9CI) → 6-Amino-N-benzyl-2-quinolone
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:9](=[O:21])[CH:8]=[CH:7]2)([O-])=O.C(C1C=CC2C(=CC=C(N)C=2)N=1)#N>>[NH2:1][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[N:10]([CH2:14][C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)[C:9](=[O:21])[CH:8]=[CH:7]2Participants
3
Procedure
The title compound (34 mg) was prepared from compound 46C in a manner similar to that described in Experiment 45C. LC/MS m/z 251 [M+H]+.
Sources & evidence
- ORD record
- ord-5b3f2ac1f4424419a38f2221d243ca20
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07405234B2
Reaction notes
Loading…