5-Isopropyl-6-(3,5-dimethylphenoxy)-2,4-pyrimidinedione → HCID 69976784, compound

HRID 581891Notes

Reaction equation

HRID 581891 reaction equation
[CH:1]([C:4]1[C:5](=[O:20])[NH:6][C:7](=[O:19])[NH:8][C:9]=1[O:10][C:11]1[CH:16]=[C:15]([CH3:17])[CH:14]=[C:13]([CH3:18])[CH:12]=1)([CH3:3])[CH3:2].C1(C)C(S(O[CH2:31][CH2:32][CH:33]2[CH2:37][CH2:36][CH2:35][CH2:34]2)(=O)=O)=CC=CC=1>>[CH2:34]1[CH2:35][CH2:36][CH2:37][CH:33]1[CH:32]([N:8]1[C:9]([O:10][C:11]2[CH:12]=[C:13]([CH3:18])[CH:14]=[C:15]([CH3:17])[CH:16]=2)=[C:4]([CH:1]([CH3:3])[CH3:2])[C:5](=[O:20])[NH:6][C:7]1=[O:19])[CH3:31]

Participants

3

Reactant 2

HCID 222565785-Isopropyl-6-(3,5-dimethylphenoxy)-2,4-pyrimidinedioneHCID 86754222HCID 86754222, compound

Product 1

HCID 69976784HCID 69976784, compoundYield 28.3%

Procedure

5-Isopropyl-6-(3,5-dimethylphenoxy)-2,4-pyrimidinedione and (2-cyclopentyl)ethyl toluenesulfonate were reacted by the same method with example 44 to obtain the titled compound (105 mg).

Sources & evidence

ORD record
ord-bc4f9a04395d4181b020e360d8f8e33c
Source dataset
uspto-grants-1999_07
Patent number
US05922727

Reaction notes

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