4-Chloro-2,5-dimethoxyaniline → HCID 59265120, compound

HRID 558343Notes

Reaction equation

HRID 558343 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.[Cl:15][C:16]1[C:22]([O:23][CH3:24])=[CH:21][C:19]([NH2:20])=[C:18]([O:25][CH3:26])[CH:17]=1>>[Cl:15][C:16]1[C:22]([O:23][CH3:24])=[CH:21][C:19]([NH:20][C:9](=[O:11])[C:8]2[CH:7]=[C:6]([CH:5]=[CH:4][C:3]=2[O:2][CH3:1])[C:12]([NH2:14])=[O:13])=[C:18]([O:25][CH3:26])[CH:17]=1

Participants

3

Reactant 2

HCID 228334-Chloro-2,5-dimethoxyanilineHCID 132228085-Carbamoyl-2-methoxybenzoic acid

Product 1

HCID 59265120HCID 59265120, compound

Procedure

The captioned compound was synthesized from 6-methoxyisophthalamic acid and 4-chloro-2,5-dimethoxyaniline by the same procedure as in the manufacturing method described in step C of Example 1-3-1.

Sources & evidence

ORD record
ord-1846e0d6aa6e4ab2ab2ad06a6dd9aef2
Source dataset
uspto-grants-2011_11
Patent number
US08063046B2

Reaction notes

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