3,4-diaminobenzenesulfonamide → HCID 178514688, compound

HRID 916747Notes

Reaction equation

HRID 916747 reaction equation
F[C:2]1[CH:16]=[CH:15][C:5]([O:6][C:7]2[CH:14]=[CH:13][C:10]([CH:11]=O)=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.[NH2:17][C:18]1[CH:19]=[C:20]([S:25]([NH2:28])(=[O:27])=[O:26])[CH:21]=[CH:22][C:23]=1[NH2:24].N[C:30]1[CH:31]=C(C=[CH:37][C:38]=1N)C(N)=O>>[CH:15]1[C:16]2[C:2](=[CH:31][CH:30]=[CH:38][CH:37]=2)[CH:3]=[CH:4][C:5]=1[O:6][C:7]1[CH:14]=[CH:13][C:10]([C:11]2[NH:24][C:23]3[CH:22]=[CH:21][C:20]([S:25]([NH2:28])(=[O:26])=[O:27])=[CH:19][C:18]=3[N:17]=2)=[CH:9][CH:8]=1

Participants

4

Reactant 3

HCID 27359273,4-diaminobenzenesulfonamideHCID 38568024-(4-Fluorophenoxy)benzaldehydeHCID 212178433,4-Diaminobenzamide

Product 1

HCID 178514688HCID 178514688, compound

Procedure

This compound was prepared according to the methods described in Example 22 and Scheme 3, substituting 4-(naphthalen-2-yloxy)-benzaldehyde for 4-(4-fluoro-phenoxy)-benzaldehyde, and 3,4-diamino-benzenesulfonamide for 3,4-diaminobenzamide.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-c615ba88cbcd442b9cad845b7ebe7027
Source dataset
uspto-grants-2007_09
Patent number
US07271261B2

Reaction notes

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