3,5-Diamino-2-methylbenzoic acid → HCID 20184489, compound

Reaction equation

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

Participants

Reactant 2

HCID 1355243,5-Diamino-2-methylbenzoic acid

HCID 121193062-Methoxy-4-[(methylsulfonyl)amino]benzoic acid

Product 1

HCID 20184489HCID 20184489, compound

Procedure

Prepared analogously to Example 14 from 4-methoxycarbonyl-1,2-phenylenediamine and 2-methoxy-4-methanesulfonylamino-benzoic acid.

Sources & evidence

ORD record: ord-b606718fbb094ff8969fa27ba813c83e
Source dataset: uspto-grants-1986_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04582837

Reaction notes

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