Phenyl(pyridin-2-yl)methanamine → 2-Phenylsulfonylamino-5-chloro-N-(phenylpyridin-2-ylmethyl)benzamide

HRID 2055820Notes

Reaction equation

HRID 2055820 reaction equation
[C:1]1([S:7]([NH:10][C:11]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:12]=2[C:13](Cl)=[O:14])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:21]1([CH:27]([NH2:34])[C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][N:29]=2)[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[C:1]1([S:7]([NH:10][C:11]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:12]=2[C:13]([NH:34][CH:27]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][N:29]=2)=[O:14])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

3

Reactant 2

HCID 2775258Phenyl(pyridin-2-yl)methanamineHCID 120832222-Phenylsulfonylamino-5-chlorobenzoyl chloride

Product 1

HCID 120832212-Phenylsulfonylamino-5-chloro-N-(phenylpyridin-2-ylmethyl)benzamide

Procedure

211 mg of the title compound were obtained from 2-phenylsulfonylamino-5-chlorobenzoyl chloride and C-phenyl-C-pyridin-2-ylmethylamine in accordance with general method 5. MS (ES+): m/z=478 (M+1).

Sources & evidence

ORD record
ord-500b54a142fd4d3a82cfd8afc10bad6b
Source dataset
uspto-grants-2008_02
Patent number
US07332608B2

Reaction notes

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