2-Oxazolidinone → 3-{5-[4-(2,4,5-Trimethylphenyl)piperazine-1-carbonyl]pyridin-2-yl}oxazolidin-2-one

HRID 1804320Notes

Reaction equation

HRID 1804320 reaction equation
Br[C:2]1[N:7]=[CH:6][C:5]([C:8]([N:10]2[CH2:15][CH2:14][N:13]([C:16]3[CH:21]=[C:20]([CH3:22])[C:19]([CH3:23])=[CH:18][C:17]=3[CH3:24])[CH2:12][CH2:11]2)=[O:9])=[CH:4][CH:3]=1.[O:25]1[CH2:29][CH2:28][NH:27][C:26]1=[O:30]>>[CH3:24][C:17]1[CH:18]=[C:19]([CH3:23])[C:20]([CH3:22])=[CH:21][C:16]=1[N:13]1[CH2:14][CH2:15][N:10]([C:8]([C:5]2[CH:4]=[CH:3][C:2]([N:27]3[CH2:28][CH2:29][O:25][C:26]3=[O:30])=[N:7][CH:6]=2)=[O:9])[CH2:11][CH2:12]1

Participants

3

Reactant 2

HCID 739492-OxazolidinoneHCID 58484642(6-Bromopyridin-3-yl)[4-(2,4,5-trimethylphenyl)piperazin-1-yl]methanone

Product 1

HCID 584844993-{5-[4-(2,4,5-Trimethylphenyl)piperazine-1-carbonyl]pyridin-2-yl}oxazolidin-2-oneYield 79%

Procedure

By reaction and treatment in the same manner as in Example 1 and using (6-bromopyridin-3-yl)[4-(2,4,5-trimethylphenyl)piperazin-1-yl]methanone (430 mg) described in Preparation Example 143 and oxazolidin-2-one (128 mg), the title compound (345 mg) was obtained.

Workup

  1. customBy reaction and treatment in the same manner as in Example 1

Sources & evidence

ORD record
ord-4748fd7bdaca4b0fa7e2203dff79b0cd
Source dataset
uspto-grants-2013_01
Patent number
US08354401B2

Reaction notes

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