Chloroacetone → HCID 15957825, compound

HRID 1611388Notes

Reaction equation

HRID 1611388 reaction equation
[CH2:1]([C:3]1[C:4](=[O:19])[NH:5][C:6](=[O:18])[NH:7][C:8]=1[O:9][C:10]1[CH:15]=[C:14]([CH3:16])[CH:13]=[C:12]([CH3:17])[CH:11]=1)[CH3:2].Cl[CH2:21][C:22](=[O:24])[CH3:23]>>[CH2:21]([N:7]1[C:8]([O:9][C:10]2[CH:11]=[C:12]([CH3:17])[CH:13]=[C:14]([CH3:16])[CH:15]=2)=[C:3]([CH2:1][CH3:2])[C:4](=[O:19])[NH:5][C:6]1=[O:18])[C:22]([CH3:23])=[O:24]

Participants

3

Reactant 2

HCID 6571ChloroacetoneHCID 109232665-Ethyl-6-(3,5-dimethylphenoxy)-2,4-pyrimidinedione

Product 1

HCID 15957825HCID 15957825, compoundYield 54%

Procedure

5-Ethyl-6-(3,5-dimethylphenoxy)-2,4-pyrimidinedione and chloroacetone were reacted by the same way with the example 1 to obtain the titled compound (172 mg, yield: 54%).

Sources & evidence

ORD record
ord-3100a8f3351e4255a48fea27b00a444e
Source dataset
uspto-grants-2006_01
Patent number
US06987114B1

Reaction notes

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