Dimethyl Sulfate → HCID 20025921, compound

HRID 1722951Notes

Reaction equation

HRID 1722951 reaction equation
[CH2:1]([C:3]1[NH:8][C:7](=[O:9])[N:6]([C:10]2[CH:15]=[C:14]([O:16][CH:17]([CH3:19])[CH3:18])[C:13]([Cl:20])=[CH:12][C:11]=2[F:21])[C:5](=[O:22])[C:4]=1[CH3:23])[CH3:2].S(OC)(O[CH3:28])(=O)=O>>[CH2:1]([C:3]1[N:8]([CH3:28])[C:7](=[O:9])[N:6]([C:10]2[CH:15]=[C:14]([O:16][CH:17]([CH3:18])[CH3:19])[C:13]([Cl:20])=[CH:12][C:11]=2[F:21])[C:5](=[O:22])[C:4]=1[CH3:23])[CH3:2]

Participants

3

Procedure

using 6-ethyl-3-(4-chloro-2-fluoro-5-isopropoxyphenyl)-5-methyl-2,4(1H,3H)-pyrimidinedione and dimethyl sulphate there is obtained 6-ethyl-3-(4-chloro-2-fluoro-5-isopropoxyphenyl)-1,5-dimethyl-2,4(1H,3H)-pyrimidinedione, m.p. 88°-91° C.;

Sources & evidence

ORD record
ord-f54d172dbb5e4f4cbb31fe7ef8d7b4de
Source dataset
uspto-grants-1989_08
Patent number
US04859229

Reaction notes

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