Benzaldehyde → HCID 3158000, compound

HRID 1767669Notes

Reaction equation

HRID 1767669 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([S:9](=[O:12])(=[O:11])[NH2:10])=[CH:4][C:3]=1[S:13]([NH2:16])(=[O:15])=[O:14].[CH:17](=O)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[C:18]1([CH:17]2[NH:1][C:2]3[CH:7]=[C:6]([Cl:8])[C:5]([S:9](=[O:11])(=[O:12])[NH2:10])=[CH:4][C:3]=3[S:13](=[O:15])(=[O:14])[NH:16]2)[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1

Participants

3

Reactant 2

HCID 240BenzaldehydeHCID 671364-Amino-6-chloro-1,3-benzenedisulfonamide

Product 1

HCID 3158000HCID 3158000, compound

Procedure

2-Amino-4-chloro-5-sulfamoylbenzenesulfonamide was transformed by Method G (using benzaldehyde). M.p. 235–238° C.

Sources & evidence

ORD record
ord-fa1948741d1d4f90bb02b13e30aa72c4
Source dataset
uspto-grants-2007_06
Patent number
US07235548B2

Reaction notes

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