(5-Methyl-1,2-oxazol-3-yl)methanol → 5-Chloro-N-[6-chloro-3-(5-methyl-3-isoxazolylmethoxy)2-pyrazinyl]-2-thiophenesulphonamide

HRID 2217977Notes

Reaction equation

HRID 2217977 reaction equation
[CH3:1][C:2]1[O:6][N:5]=[C:4]([CH2:7][OH:8])[CH:3]=1.[Cl:9][C:10]1[S:14][C:13]([S:15]([NH:18][C:19]2[C:24](Br)=[N:23][CH:22]=[C:21]([Cl:26])[N:20]=2)(=[O:17])=[O:16])=[CH:12][CH:11]=1>>[Cl:9][C:10]1[S:14][C:13]([S:15]([NH:18][C:19]2[C:24]([O:8][CH2:7][C:4]3[CH:3]=[C:2]([CH3:1])[O:6][N:5]=3)=[N:23][CH:22]=[C:21]([Cl:26])[N:20]=2)(=[O:17])=[O:16])=[CH:12][CH:11]=1

Participants

3

Reactant 2

HCID 2736567(5-Methyl-1,2-oxazol-3-yl)methanolHCID 102159965-Chloro-N-(3-bromo-6-chloro-2-pyrazinyl)-2-thiophenesulphonamide

Product 1

HCID 597694605-Chloro-N-[6-chloro-3-(5-methyl-3-isoxazolylmethoxy)2-pyrazinyl]-2-thiophenesulphonamide

Procedure

Prepared by the method of Example 20b using (5-methyl-3-isoxazolyl)methanol and 5-chloro-N-(3-bromo-6-chloro-2-pyrazinyl)-2-thiophenesulphonamide.

Workup

  1. customPrepared by the method of Example 20b

Sources & evidence

ORD record
ord-23f1792b676c4ed0962ed9ef9e92bb56
Source dataset
uspto-grants-2008_08
Patent number
US07410972B2

Reaction notes

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