1-Methylimidazolidin-2-one → HCID 71252111, compound

HRID 2411792Notes

Reaction equation

HRID 2411792 reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]([C:10]([N:12]2[CH2:17][CH2:16][N:15]([C:18]3[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][C:19]=3[CH3:25])[CH2:14][CH2:13]2)=[O:11])=[C:6]([CH:9]=1)[C:7]#[N:8].[CH3:26][N:27]1[CH2:31][CH2:30][NH:29][C:28]1=[O:32]>>[CH3:25][C:19]1[CH:20]=[C:21]([CH3:24])[CH:22]=[CH:23][C:18]=1[N:15]1[CH2:16][CH2:17][N:12]([C:10]([C:5]2[CH:4]=[CH:3][C:2]([N:29]3[CH2:30][CH2:31][N:27]([CH3:26])[C:28]3=[O:32])=[CH:9][C:6]=2[C:7]#[N:8])=[O:11])[CH2:13][CH2:14]1

Participants

3

Reactant 2

HCID 5676001-Methylimidazolidin-2-oneHCID 71251979HCID 71251979, compound

Product 1

HCID 71252111HCID 71252111, compoundYield 83.7%

Procedure

Using 5-bromo-2-[4-(2,4-dimethylphenyl)piperazine-1-carbonyl]benzonitrile (398 mg) described in Preparation Example 188 and 1-methylimidazolidin-2-one (120 mg) and by the reaction and treatment in the same manner as in Example 1, the title compound (349 mg) was obtained.

Sources & evidence

ORD record
ord-d86e8bb450b34ae28646afdb98c75f5d
Source dataset
uspto-grants-2014_08
Patent number
US08816079B2

Reaction notes

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