Potassium Carbonate → 2-[3-Chloro-2-(methylsulfonylaminocarbonyl)phenoxy]-4,6-dimethoxy-1,3,5-triazine

HRID 1885972Notes

Reaction equation

HRID 1885972 reaction equation
[Cl:1][C:2]1[CH:19]=[CH:18][CH:17]=[C:16]([O:20][C:21]2[N:26]=[C:25]([O:27][CH3:28])[N:24]=[C:23]([O:29][CH3:30])[N:22]=2)[C:3]=1[C:4](OC1C=CC([N+]([O-])=O)=CC=1)=[O:5].[CH3:31][S:32]([NH2:35])(=[O:34])=[O:33].C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[Cl:1][C:2]1[C:3]([C:4]([NH:35][S:32]([CH3:31])(=[O:34])=[O:33])=[O:5])=[C:16]([CH:17]=[CH:18][CH:19]=1)[O:20][C:21]1[N:26]=[C:25]([O:27][CH3:28])[N:24]=[C:23]([O:29][CH3:30])[N:22]=1

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 72879MethanesulfonamideHCID 198765984-Nitrophenyl 2-chloro-6-(4,6-dimethoxy-1,3,5-triazin-2-yloxy)benzoate

Product 1

HCID 198765852-[3-Chloro-2-(methylsulfonylaminocarbonyl)phenoxy]-4,6-dimethoxy-1,3,5-triazine

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

This compound is prepared in a manner analogous to that of Example 1, Step I, using equimolar amounts of 4-nitrophenyl 2-chloro-6-(4,6-dimethoxy-1,3,5-triazin-2-yloxy)benzoate, methanesulfonamide, and potassium carbonate in acetonitrile to yield 2-[3-chloro-2-(methylsulfonylaminocarbonyl)phenoxy]-4,6-dimethoxy-1,3,5-triazine, Compound 38 of Table 1.

Workup

  1. customThis compound is prepared in a manner analogous to that of Example 1, Step I

Sources & evidence

ORD record
ord-dd503b8761c34973817f58b1c0ee42ef
Source dataset
uspto-grants-1992_09
Patent number
US05149357

Reaction notes

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