2-(Chloromethyl)quinoline → 6-(3,5-Dimethylbenzoyl)-5-isopropyl-1-(2-quinolylmethyl)pyrimidine-2,4-dione

HRID 1611368Notes

Reaction equation

HRID 1611368 reaction equation
[CH:1]([C:4]1[C:5](=[O:21])[NH:6][C:7](=[O:20])[NH:8][C:9]=1[C:10](=[O:19])[C:11]1[CH:16]=[C:15]([CH3:17])[CH:14]=[C:13]([CH3:18])[CH:12]=1)([CH3:3])[CH3:2].Cl[CH2:23][C:24]1[CH:33]=[CH:32][C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[N:25]=1>>[N:25]1[C:26]2[C:31](=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:32]=[CH:33][C:24]=1[CH2:23][N:8]1[C:9]([C:10](=[O:19])[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:21])[NH:6][C:7]1=[O:20]

Participants

3

Reactant 2

HCID 203942-(Chloromethyl)quinolineHCID 222565826-(3,5-Dimethyl-benzoyl)-5-isopropyl-1H-pyrimidine-2,4-dione

Product 1

HCID 159578086-(3,5-Dimethylbenzoyl)-5-isopropyl-1-(2-quinolylmethyl)pyrimidine-2,4-dioneYield 39.8%

Procedure

5-Isopropyl-6-(3,5-dimethylbenzoyl)-2,4-pyrimidinedione and 2-chloromethyl quinoline were reacted by the same way with the example 1 to obtain the titled compound (170 mg, yield: 39.8%).

Sources & evidence

ORD record
ord-2f45f929dbe041b0b8f55676382c7160
Source dataset
uspto-grants-2006_01
Patent number
US06987114B1

Reaction notes

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