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

HRID 1804283Notes

Reaction equation

HRID 1804283 reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]([C:13]([N:15]2[CH2:20][CH2:19][N:18]([C:21]3[C:26]([CH3:27])=[CH:25][C:24]([CH3:28])=[CH:23][N:22]=3)[CH2:17][CH2:16]2)=[O:14])=[C:6]([NH:8][S:9]([CH3:12])(=[O:11])=[O:10])[CH:7]=1.[O:29]1[CH2:33][CH2:32][NH:31][C:30]1=[O:34]>>[CH3:27][C:26]1[C:21]([N:18]2[CH2:19][CH2:20][N:15]([C:13]([C:5]3[CH:4]=[CH:3][C:2]([N:31]4[CH2:32][CH2:33][O:29][C:30]4=[O:34])=[CH:7][C:6]=3[NH:8][S:9]([CH3:12])(=[O:11])=[O:10])=[O:14])[CH2:16][CH2:17]2)=[N:22][CH:23]=[C:24]([CH3:28])[CH:25]=1

Participants

3

Reactant 2

HCID 739492-OxazolidinoneHCID 58484868N-{5-bromo-2-[4-(3,5-dimethylpyridin-2-yl)piperazine-1-carbonyl]phenyl}methanesulfonamide

Product 1

HCID 584844833-{4-[4-(3,5-Dimethylpyridin-2-yl)piperazine-1-carbonyl]-3-methanesulfonylaminophenyl}oxazolidin-2-oneYield 17.8%

Procedure

By reaction and treatment in the same manner as in Example 1 and using [N-{5-bromo-2-[4-(3,5-dimethylpyridin-2-yl)piperazine-1-carbonyl]phenyl}methanesulfonamide (321 mg) described in Preparation Example 123 and oxazolidin-2-one (59.8 mg), the title compound (57.8 mg) was obtained.

Workup

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

Sources & evidence

ORD record
ord-28c15aca93f3428080b42ded002d9b48
Source dataset
uspto-grants-2013_01
Patent number
US08354401B2

Reaction notes

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