Reaction equation
I[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[NH:14]1[C:22]2[C:17](=[CH:18][C:19]([CH2:23][N:24]3[CH2:29][CH2:28][CH:27]([C:30]4[CH:31]=[C:32]([NH:36][C:37](=[O:41])[CH:38]([CH3:40])[CH3:39])[CH:33]=[CH:34][CH:35]=4)[CH2:26][CH2:25]3)=[CH:20][CH:21]=2)[CH:16]=[CH:15]1>>[C:3]1([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[N:14]1[C:22]2[C:17](=[CH:18][C:19]([CH2:23][N:24]3[CH2:29][CH2:28][CH:27]([C:30]4[CH:31]=[C:32]([NH:36][C:37](=[O:41])[CH:38]([CH3:39])[CH3:40])[CH:33]=[CH:34][CH:35]=4)[CH2:26][CH2:25]3)=[CH:20][CH:21]=2)[CH:16]=[CH:15]1Participants
3
Procedure
Prepared by Procedure C and Scheme Q1, with CuBr in place of Cu, using 2-iodo-1,1′-biphenyl and N-{3-[1-(1H-indol-5-ylmethyl)-4-piperidinyl]phenyl}-2-methylpropanamide: ESMS m/e: 528.3 (M+H)+.
Sources & evidence
- ORD record
- ord-14935a64e963447396d8594dd4d4c36e
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727264B1
Linked notes
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