Azetidine → 1-Azetidin-1-yl-6-methoxy-4-phenylisoquinoline-3-carbonitrile
Reaction equation
[CH2:1]([NH:4][C:5]1[C:14]2[C:9](=[CH:10][C:11]([O:15][CH3:16])=[CH:12][CH:13]=2)[C:8]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[C:7]([C:23]#[N:24])[N:6]=1)[CH:2]=[CH2:3].N1CCC1>>[N:4]1([C:5]2[C:14]3[C:9](=[CH:10][C:11]([O:15][CH3:16])=[CH:12][CH:13]=3)[C:8]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[C:7]([C:23]#[N:24])[N:6]=2)[CH2:3][CH2:2][CH2:1]1Participants
3
Procedure
Following the procedure for 1-(allylamino)-6-methoxy-4-phenylisoquinoline-3-carbonitrile, using azetidine in place of allylamine, the title compound was synthesized.
Sources & evidence
- ORD record
- ord-a317926076b44fe887e35360cd965e16
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07691879B2
Reaction notes
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