2-Aminoquinoline → HCID 59265181, compound

HRID 646341Notes

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][C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[N:17]=1>>[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][C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[N:17]=1)=[O:11]

Participants

Reactant 2

HCID 113792-Aminoquinoline

HCID 132228085-Carbamoyl-2-methoxybenzoic acid

Product 1

HCID 59265181HCID 59265181, compound

Procedure

The captioned compound was synthesized from 6-methoxyisophthalamic acid and 2-aminoquinoline by the same procedure as in the manufacturing method described in step C of Example 1-3-1.

Sources & evidence

ORD record: ord-a042425b672947d79a0b30f05f50bfbc
Source dataset: uspto-grants-2010_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07705053B2

Reaction notes

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