(S)-5-(Hydroxymethyl)-2-pyrrolidinone → HCID 71252443, compound

HRID 2411674Notes

Reaction equation

HRID 2411674 reaction equation
[OH:1][CH2:2][C@H:3]1[NH:7][C:6](=[O:8])[CH2:5][CH2:4]1.Br[C:10]1[CH:15]=[CH:14][C:13]([C:16]([N:18]2[CH2:23][CH2:22][N:21]([C:24]3[C:29]([CH3:30])=[CH:28][C:27]([CH3:31])=[CH:26][N:25]=3)[CH2:20][CH2:19]2)=[O:17])=[C:12]([CH3:32])[CH:11]=1>>[CH3:30][C:29]1[C:24]([N:21]2[CH2:20][CH2:19][N:18]([C:16]([C:13]3[CH:14]=[CH:15][C:10]([N:7]4[C@H:3]([CH2:2][OH:1])[CH2:4][CH2:5][C:6]4=[O:8])=[CH:11][C:12]=3[CH3:32])=[O:17])[CH2:23][CH2:22]2)=[N:25][CH:26]=[C:27]([CH3:31])[CH:28]=1

Participants

3

Reactant 2

HCID 643511(S)-5-(Hydroxymethyl)-2-pyrrolidinoneHCID 58484835(4-Bromo-2-methylphenyl)[4-(3,5-dimethylpyridin-2-yl)piperazin-1-yl]methanone

Product 1

HCID 71252443HCID 71252443, compoundYield 17.6%

Procedure

Using (S)-5-hydroxymethylpyrrolidin-2-one (168 mg) and (4-bromo-2-methylphenyl) [4-(3,5-dimethylpyridin-2-yl)piperazin-1-yl]methanone (516 mg) described in Preparation Example 118 and by the reaction and treatment in the same manner as in Example 1, the title compound (99 mg) was obtained.

Workup

  1. customdescribed in Preparation Example 118 and by the reaction and treatment in the same manner as in Example 1

Sources & evidence

ORD record
ord-8069f780aa9e4b31941ed00d87cbeecb
Source dataset
uspto-grants-2014_08
Patent number
US08816079B2

Reaction notes

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