(3-Methylpyridin-2-yl)methanol → HCID 59168123, compound

HRID 1443960Notes

Reaction equation

HRID 1443960 reaction equation
[CH3:1][C:2]1[C:3]([CH2:8][OH:9])=[N:4][CH:5]=[CH:6][CH:7]=1.Br[C:11]1[C:12]([NH:18][S:19]([C:22]2[CH:27]=[CH:26][CH:25]=[C:24]([Cl:28])[C:23]=2[Cl:29])(=[O:21])=[O:20])=[N:13][CH:14]=[C:15]([CH3:17])[N:16]=1>>[Cl:29][C:23]1[C:24]([Cl:28])=[CH:25][CH:26]=[CH:27][C:22]=1[S:19]([NH:18][C:12]1[C:11]([O:9][CH2:8][C:3]2[C:2]([CH3:1])=[CH:7][CH:6]=[CH:5][N:4]=2)=[N:16][C:15]([CH3:17])=[CH:14][N:13]=1)(=[O:20])=[O:21]

Participants

3

Reactant 2

HCID 1514369(3-Methylpyridin-2-yl)methanolHCID 59168147N-(3-Bromo-5-methyl-2-pyrazinyl)-2,3-dichlorobenzenesulphonamide

Product 1

HCID 59168123HCID 59168123, compound

Procedure

Prepared by the method of Example 20 using 3-methylpyridine-2-methanol (0.05 g) and N-(3-bromo-5-methyl-2-pyrazinyl)-2,3-dichlorobenzenesulphonamide (0.1 g). Yield 0.021 g.

Sources & evidence

ORD record
ord-102488e7ee4b43f68c2ddef4c0e5fa60
Source dataset
uspto-grants-2010_02
Patent number
US07662825B2

Reaction notes

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