(5-Methyl-1,2-oxazol-3-yl)methanol → HCID 10194766, compound

HRID 1443955Notes

Reaction equation

HRID 1443955 reaction equation
[CH3:1][C:2]1[O:6][N:5]=[C:4]([CH2:7][OH:8])[CH:3]=1.Br[C:10]1[C:11]([NH:17][S:18]([C:21]2[CH:26]=[CH:25][CH:24]=[C:23]([Cl:27])[C:22]=2[Cl:28])(=[O:20])=[O:19])=[N:12][CH:13]=[C:14]([CH3:16])[N:15]=1>>[Cl:28][C:22]1[C:23]([Cl:27])=[CH:24][CH:25]=[CH:26][C:21]=1[S:18]([NH:17][C:11]1[C:10]([O:8][CH2:7][C:4]2[CH:3]=[C:2]([CH3:1])[O:6][N:5]=2)=[N:15][C:14]([CH3:16])=[CH:13][N:12]=1)(=[O:19])=[O:20]

Participants

3

Reactant 2

HCID 2736567(5-Methyl-1,2-oxazol-3-yl)methanolHCID 59168147N-(3-Bromo-5-methyl-2-pyrazinyl)-2,3-dichlorobenzenesulphonamide

Product 1

HCID 10194766HCID 10194766, compound

Procedure

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

Sources & evidence

ORD record
ord-d3976b63f3b544a4b3feccb8a87c1f6b
Source dataset
uspto-grants-2010_02
Patent number
US07662825B2

Reaction notes

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