4-(2-Aminoethyl)benzenesulfonamide → HCID 58808581, compound

HRID 1921507Notes

Reaction equation

HRID 1921507 reaction equation
[CH2:1]([C:3]1[C:8](=[O:9])[NH:7][C:6]([CH3:10])=[C:5]([C:11]2[CH:12]=[N:13][CH:14]=[C:15]([C:17]([OH:19])=O)[CH:16]=2)[CH:4]=1)[CH3:2].[S:20]([C:24]1[CH:29]=[CH:28][C:27]([CH2:30][CH2:31][NH2:32])=[CH:26][CH:25]=1)(=[O:23])(=[O:22])[NH2:21]>>[S:20]([C:24]1[CH:25]=[CH:26][C:27]([CH2:30][CH2:31][NH:32][C:17]([C:15]2[CH:16]=[C:11]([C:5]3[CH:4]=[C:3]([CH2:1][CH3:2])[C:8](=[O:9])[NH:7][C:6]=3[CH3:10])[CH:12]=[N:13][CH:14]=2)=[O:19])=[CH:28][CH:29]=1)(=[O:22])(=[O:23])[NH2:21]

Participants

3

Reactant 2

HCID 1696824-(2-Aminoethyl)benzenesulfonamideHCID 588087025'-Ethyl-2'-methyl-6'-oxo-1',6'-dihydro-[3,3']bipyridinyl-5-carboxylic acid

Product 1

HCID 58808581HCID 58808581, compound

Procedure

Method 1, Example 205 is substantially repeated except for utilizing 5′-ethyl-2′-methyl-6′-oxo-1′,6′-dihydro-[3,3′]bipyridinyl-5-carboxylic acid and 2-(4-sulfamoyl-phenyl)-ethyl-amine to afford the title compound. MS: m/e=441 (M+H).

Sources & evidence

ORD record
ord-3bc3908ef9ce4ce9b21fb5c351b032d7
Source dataset
uspto-grants-2012_05
Patent number
US08173682B2

Reaction notes

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