HCID 21506007, compound → 3-Amino-4-(2-methylanilino)-5-sulfamoylbenzoic acid

HRID 1287727Notes

Reaction equation

HRID 1287727 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([S:21](=[O:24])(=[O:23])[NH2:22])[C:12]=1[NH:13][C:14]1[C:15]([CH3:20])=[CH:16][CH:17]=[CH:18][CH:19]=1)[C:7]([OH:9])=[O:8])([O-])=O.N(C1C(S(=O)(=O)N)=CC(C(O)=O)=CC=1[N+]([O-])=O)C1C=CC=CC=1>>[NH2:1][C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([S:21](=[O:24])(=[O:23])[NH2:22])[C:12]=1[NH:13][C:14]1[C:15]([CH3:20])=[CH:16][CH:17]=[CH:18][CH:19]=1)[C:7]([OH:9])=[O:8]

Participants

3

Reactant 2

HCID 21506007HCID 21506007, compoundHCID 215060714-Anilino-3-nitro-5-sulphamyl-benzoic acid

Product 1

HCID 215061493-Amino-4-(2-methylanilino)-5-sulfamoylbenzoic acid

Procedure

By substituting 3-nitro-5-sulphamyl-4(o-toluidino)-benzoic acid for the 4-anilino-3-nitro-5-sulphamyl-benzoic acid of Example 9 B, the above compound was obtained.

Workup

  1. customthe above compound was obtained

Sources & evidence

ORD record
ord-31f75e13f4d840d599f6138562295f57
Source dataset
uspto-grants-1976_10
Patent number
US03985777

Reaction notes

Loading…