Methanesulfonamide → HCID 53799918, compound

HRID 1458576Notes

Reaction equation

HRID 1458576 reaction equation
[NH2:1][C:2]1[C:11]([CH2:12][CH3:13])=[C:10]([Cl:14])[CH:9]=[C:8]2[C:3]=1[N:4]=[C:5]([O:17][CH3:18])[C:6]([O:15][CH3:16])=[N:7]2.[CH3:19][S:20](N)(=[O:22])=[O:21]>>[Cl:14][C:10]1[CH:9]=[C:8]2[C:3]([N:4]=[C:5]([O:17][CH3:18])[C:6]([O:15][CH3:16])=[N:7]2)=[C:2]([NH:1][S:20]([CH3:19])(=[O:22])=[O:21])[C:11]=1[CH2:12][CH3:13]

Participants

3

Reactant 2

HCID 72879MethanesulfonamideHCID 54190583HCID 54190583, compound

Product 1

HCID 53799918HCID 53799918, compoundYield 47%

Procedure

5-Amino-7-chloro-6-ethyl-2,3-dimethoxyquinoxaline was converted to the methane sulphonamide derivative by the method of step (g) above. The product was obtained in 47% yield.

Workup

  1. customThe product was obtained in 47% yield

Sources & evidence

ORD record
ord-5b67fa1544dd4ee7aa9cdc94999a4715
Source dataset
uspto-grants-1998_12
Patent number
US05852016

Reaction notes

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