4-Amino-1-(2-naphthyl)methylpiperidine → 7-methoxy-4-(2-methoxyphenyl)-N-[1-(naphthalen-2-ylmethyl)piperidin-4-yl]phthalazin-1-amine
Reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[CH:10]=2)[C:5]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[O:20][CH3:21])=[N:4][N:3]=1.[NH2:22][CH:23]1[CH2:28][CH2:27][N:26]([CH2:29][C:30]2[CH:39]=[CH:38][C:37]3[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=3)[CH:31]=2)[CH2:25][CH2:24]1>>[CH3:13][O:12][C:9]1[CH:10]=[C:11]2[C:6]([C:5]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[O:20][CH3:21])=[N:4][N:3]=[C:2]2[NH:22][CH:23]2[CH2:24][CH2:25][N:26]([CH2:29][C:30]3[CH:39]=[CH:38][C:37]4[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=4)[CH:31]=3)[CH2:27][CH2:28]2)=[CH:7][CH:8]=1Participants
3
Procedure
This compound is obtained according to the procedure described in 1.4. by reacting 1-chloro-7-methoxy-4-(2-methoxyphenyl)phthalazine described with 4-amino-1-(naphthalen-2-ylmethyl)piperidine.
Workup
- customThis compound is obtained
Sources & evidence
- ORD record
- ord-231fdff379a54365910539ecabb96ed9
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07423030B2
Reaction notes
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