Methyl iodide → HCID 21265589, compound

HRID 1722953Notes

Reaction equation

HRID 1722953 reaction equation
[Br:1][C:2]1[C:7]([O:8][CH:9]([CH3:11])[CH3:10])=[CH:6][C:5]([N:12]2[C:17](=[O:18])[CH:16]=[C:15]([C:19]([F:22])([F:21])[F:20])[NH:14][C:13]2=[O:23])=[C:4]([F:24])[CH:3]=1.[C:25](=O)([O-])[O-].[K+].[K+].CI>C(#N)C>[Br:1][C:2]1[C:7]([O:8][CH:9]([CH3:11])[CH3:10])=[CH:6][C:5]([N:12]2[C:17](=[O:18])[CH:16]=[C:15]([C:19]([F:22])([F:21])[F:20])[N:14]([CH3:25])[C:13]2=[O:23])=[C:4]([F:24])[CH:3]=1

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 20025935HCID 20025935, compound

Product 1

HCID 21265589HCID 21265589, compound

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

using 3-(4-bromo-2-fluoro-5-isopropoxyphenyl)-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione with potassium carbonate and methyl iodide in acetonitrile there is obtained 3-(4-bromo-2-fluoro-5-isopropoxyphenyl)-1-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione, m.p. 79° C.;

Sources & evidence

ORD record
ord-c81af585fef74f9bb951e8ebda886ca8
Source dataset
uspto-grants-1989_08
Patent number
US04859229

Reaction notes

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