P-Anisidine → HCID 73386762, compound

HRID 1480764Notes

Reaction equation

HRID 1480764 reaction equation
[CH3:1][O:2][C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[CH:5][CH:4]=1.Cl[C:11]1[N:12]=[CH:13][C:14]2[C:19]([CH:20]=1)=[C:18]([C:21]1[CH:22]=[N:23][N:24]([CH3:26])[CH:25]=1)[CH:17]=[CH:16][CH:15]=2>>[CH3:1][O:2][C:3]1[CH:9]=[CH:8][C:6]([NH:7][C:11]2[N:12]=[CH:13][C:14]3[C:19]([CH:20]=2)=[C:18]([C:21]2[CH:22]=[N:23][N:24]([CH3:26])[CH:25]=2)[CH:17]=[CH:16][CH:15]=3)=[CH:5][CH:4]=1

Participants

3

Reactant 2

HCID 7732P-AnisidineHCID 90000510HCID 90000510, compound

Product 1

HCID 73386762HCID 73386762, compound

Procedure

The title compound was prepared according to Method 3 (Example 27) using 4-methoxyaniline and 3-Chloro-5-(1-methyl-1H-pyrazol-4-yl)isoquinoline (Preparation 7).

Sources & evidence

ORD record
ord-83a44d62072e4869a848f900572008cb
Source dataset
uspto-grants-2016_08
Patent number
US09409907B2

Reaction notes

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