4-Phenylbutanoyl Chloride → HCID 86607723, compound

HRID 1622140Notes

Reaction equation

HRID 1622140 reaction equation
[CH:1]([C:3]1[CH:4]=[C:5]([S:20]([NH2:23])(=[O:22])=[O:21])[CH:6]=[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[CH:12]=2)[C:8]=1[O:9][CH3:10])=[O:2].[C:24]1([CH2:30][CH2:31][CH2:32][C:33](Cl)=[O:34])[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[CH:1]([C:3]1[CH:4]=[C:5]([S:20]([NH:23][C:33](=[O:34])[CH2:32][CH2:31][CH2:30][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)(=[O:22])=[O:21])[CH:6]=[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[CH:12]=2)[C:8]=1[O:9][CH3:10])=[O:2]

Participants

3

Reactant 2

HCID 117898654-Phenylbutanoyl ChlorideHCID 866077105-Formyl-6-methoxy-3'-nitro-biphenyl-3-sulfonamide

Product 1

HCID 86607723HCID 86607723, compound

Procedure

Proceeding as in Reference 21, but substituting 5-formyl-6-methoxy-3′-nitro-biphenyl-3-sulfonamide and 4-phenylbutyryl chloride, gave 5-formyl-6-methoxy-3′-nitro-N-(4-phenylbutyryl)-biphenyl-3-sulfonamide.

Sources & evidence

ORD record
ord-a82e2962f0d54c32ade2e2e3cf687145
Source dataset
uspto-grants-2014_07
Patent number
US08778625B2

Reaction notes

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