Dimethyl Sulfate → HCID 21270791, compound
Reaction equation
[Cl:1][C:2]1[C:7]([OH:8])=[CH:6][C:5]([N:9]2[C:14](=[O:15])[CH:13]=[C:12]([C:16]([F:22])([F:21])[C:17]([F:20])([F:19])[F:18])[N:11]=[C:10]2[O:23][CH2:24][CH3:25])=[C:4]([F:26])[CH:3]=1.S(OC)(O[CH3:31])(=O)=O.C(=O)([O-])[O-].[Na+].[Na+]>CC(C)=O>[CH2:24]([O:23][C:10]1[N:9]([C:5]2[CH:6]=[C:7]([O:8][CH3:31])[C:2]([Cl:1])=[CH:3][C:4]=2[F:26])[C:14](=[O:15])[CH:13]=[C:12]([C:16]([F:21])([F:22])[C:17]([F:20])([F:18])[F:19])[N:11]=1)[CH3:25]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
using 1-(4-chloro-2-fluoro-5-hydroxyphenyl)-2-ethoxy-4-pentafluoroethyl-6(1H)-pyrimidinone and dimethyl sulphate with sodium carbonate in acetone there is obtained 2-ethoxy-1-(4-chloro-2-fluoro-5 -methoxyphenyl)-4-pentafluoroethyl-6(1H)-pyrimidinone, 1H-NMR (CDCl3, 400 MHz): 7.33 ppm (d,1H), 6.79 ppm (d,1H), 6.65 ppm (s,1H), 4.48 ppm (m,2H), 3.89 ppm (s,3H), 1.29 ppm (t,3H);
Sources & evidence
- ORD record
- ord-afe37d5888944c698cf4c4db5fa9ad54
- Source dataset
- uspto-grants-1989_03
- Patent number
- US04812164
Reaction notes
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