5-Aminoquinoline → HCID 11484062, compound

HRID 646330Notes

Reaction equation

HRID 646330 reaction equation
[CH3:1][O:2][C:3]1[C:8]([C:9]([OH:11])=O)=[CH:7][C:6]([C:12]([NH2:14])=[O:13])=[CH:5][CH:4]=1.[NH2:15][C:16]1[CH:25]=[CH:24][CH:23]=[C:22]2[C:17]=1[CH:18]=[CH:19][CH:20]=[N:21]2>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:12]([NH2:14])=[O:13])=[CH:7][C:8]=1[C:9]([NH:15][C:16]1[CH:25]=[CH:24][CH:23]=[C:22]2[C:17]=1[CH:18]=[CH:19][CH:20]=[N:21]2)=[O:11]

Participants

3

Reactant 2

HCID 119115-AminoquinolineHCID 132228085-Carbamoyl-2-methoxybenzoic acid

Product 1

HCID 11484062HCID 11484062, compound

Procedure

The captioned compound was synthesized from 6-methoxyisophthalamic acid and 5-aminoquinoline by the same procedure as in the manufacturing method described in step C of Example 1-3-1.

Sources & evidence

ORD record
ord-5ce6410824fd4a2d9577548203d1b102
Source dataset
uspto-grants-2010_04
Patent number
US07705053B2

Reaction notes

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