Dimethyl Sulfate → HCID 20026132, compound
Reaction equation
[CH2:1]([C:3]1[C:4](=[O:23])[N:5]([C:11]2[CH:16]=[C:15]([O:17][CH:18]([CH3:20])[CH3:19])[C:14]([Cl:21])=[CH:13][C:12]=2[F:22])[C:6](=[O:10])[NH:7][C:8]=1[CH3:9])[CH3:2].S(OC)(O[CH3:28])(=O)=O>>[CH2:1]([C:3]1[C:4](=[O:23])[N:5]([C:11]2[CH:16]=[C:15]([O:17][CH:18]([CH3:19])[CH3:20])[C:14]([Cl:21])=[CH:13][C:12]=2[F:22])[C:6](=[O:10])[N:7]([CH3:28])[C:8]=1[CH3:9])[CH3:2]Participants
3
Procedure
using 5-ethyl-3-(4-chloro-2-fluoro-5-isopropoxyphenyl)-6-methyl-2,4(1H,3H)-pyrimidinedione and dimethyl sulphate there is obtained 5-ethyl-3-(4-chloro-2-fluoro-5-isopropoxyphenyl)-1,6-dimethyl-2,4(1H,3H)-pyrimidinedione, m.p. 124°-125° C.;
Sources & evidence
- ORD record
- ord-f9fe326f99714cd596fd3a356d6546e6
- Source dataset
- uspto-grants-1989_08
- Patent number
- US04859229
Reaction notes
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