4-Amino-1-(2-naphthyl)methylpiperidine → 5,7-dimethoxy-4-ethyl-N-[1-(naphthalen-2-ylmethyl)piperidin-4-yl]phthalazin-1-amine

HRID 29973Notes

Reaction equation

HRID 29973 reaction equation
Cl[C:2]1[C:11]2[C:6](=[C:7]([O:14][CH3:15])[CH:8]=[C:9]([O:12][CH3:13])[CH:10]=2)[C:5]([CH2:16][CH3:17])=[N:4][N:3]=1.[NH2:18][CH:19]1[CH2:24][CH2:23][N:22]([CH2:25][C:26]2[CH:35]=[CH:34][C:33]3[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=3)[CH:27]=2)[CH2:21][CH2:20]1>>[CH3:15][O:14][C:7]1[CH:8]=[C:9]([O:12][CH3:13])[CH:10]=[C:11]2[C:6]=1[C:5]([CH2:16][CH3:17])=[N:4][N:3]=[C:2]2[NH:18][CH:19]1[CH2:20][CH2:21][N:22]([CH2:25][C:26]2[CH:35]=[CH:34][C:33]3[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=3)[CH:27]=2)[CH2:23][CH2:24]1

Participants

3

Reactant 2

HCID 111958234-Amino-1-(2-naphthyl)methylpiperidineHCID 866122191-Chloro-5,7-dimethoxy-4-ethylphthalazine

Product 1

HCID 692140475,7-dimethoxy-4-ethyl-N-[1-(naphthalen-2-ylmethyl)piperidin-4-yl]phthalazin-1-amine

Procedure

This compound is obtained according to the procedure described in 1.4. by reacting 1-chloro-5,7-dimethoxy-4-ethylphthalazine with 4-amino-1-(naphthalen-2-yl-methyl)piperidine.

Workup

  1. customThis compound is obtained

Sources & evidence

ORD record
ord-f86339f9c01247518d78dbcd7210e3b5
Source dataset
uspto-grants-2008_09
Patent number
US07423030B2

Reaction notes

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