1-Benzyl-4-piperidylamine → N-(1-benzylpiperidin-4-yl)-7-methoxy-4-(5-methylthiophen-2-yl)phthalazin-1-amine

HRID 29936

Reaction equation

HRID 29936 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[S:15][C:16]([CH3:19])=[CH:17][CH:18]=2)=[N:4][N:3]=1.[NH2:20][CH:21]1[CH2:26][CH2:25][N:24]([CH2:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[CH2:23][CH2:22]1>>[CH2:27]([N:24]1[CH2:25][CH2:26][CH:21]([NH:20][C:2]2[C:11]3[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[CH:10]=3)[C:5]([C:14]3[S:15][C:16]([CH3:19])=[CH:17][CH:18]=3)=[N:4][N:3]=2)[CH2:22][CH2:23]1)[C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1

Participants

3

Reactant 2

HCID 4158521-Benzyl-4-piperidylamineHCID 866122111-Chloro-7-methoxy-4-(5-methylthiophen-2-yl)phthalazine

Product 1

HCID 69209324N-(1-benzylpiperidin-4-yl)-7-methoxy-4-(5-methylthiophen-2-yl)phthalazin-1-amine

Procedure

This compound is obtained according to the procedure described in 1.4. by reacting 1-chloro-7-methoxy-4-(5-methylthiophen-2-yl)phthalazine with 4-amino-1-benzylpiperidine.

Workup

  1. customThis compound is obtained

Sources & evidence

ORD record
ord-ecd619d2bb514c7381c728f3797674d9
Source dataset
uspto-grants-2008_09
Patent number
US07423030B2

Linked notes

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