P-Anisidine → 4-Methoxy-N-(4-sulfamoylbenzylidene)aniline

HRID 856839Notes

Reaction equation

HRID 856839 reaction equation
[S:1]([C:5]1[CH:12]=[CH:11][C:8]([CH:9]=O)=[CH:7][CH:6]=1)(=[O:4])(=[O:3])[NH2:2].[CH3:13][O:14][C:15]1[CH:21]=[CH:20][C:18]([NH2:19])=[CH:17][CH:16]=1>>[CH3:13][O:14][C:15]1[CH:21]=[CH:20][C:18]([N:19]=[CH:9][C:8]2[CH:11]=[CH:12][C:5]([S:1](=[O:4])(=[O:3])[NH2:2])=[CH:6][CH:7]=2)=[CH:17][CH:16]=1

Participants

3

Reactant 2

HCID 7732P-AnisidineHCID 1510884-Sulfamoylbenzaldehyde

Product 1

HCID 218627504-Methoxy-N-(4-sulfamoylbenzylidene)aniline

Procedure

Following a procedure similar to that described in Example 1(i), but using 4-sulfamoylbenzaldehyde and 4-methoxyaniline as starting materials, the title compound was obtained as a pale yellow powder (yield 85%).

Sources & evidence

ORD record
ord-6cb093e6962e45fdb092374e34d44826
Source dataset
uspto-grants-2006_12
Patent number
USRE039420E1

Reaction notes

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