2-Oxazolidinone, 5,5-dimethyl- → HCID 58484544, compound

HRID 1804259Notes

Reaction equation

HRID 1804259 reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([C:8]([N:10]2[CH2:15][CH2:14][N:13]([C:16]3[C:21]([CH2:22][CH3:23])=[CH:20][C:19]([CH3:24])=[CH:18][N:17]=3)[CH2:12][CH2:11]2)=[O:9])=[C:4]([F:25])[CH:3]=1.[CH3:26][C:27]1([CH3:33])[O:31][C:30](=[O:32])[NH:29][CH2:28]1>>[CH2:22]([C:21]1[C:16]([N:13]2[CH2:14][CH2:15][N:10]([C:8]([C:5]3[CH:6]=[CH:7][C:2]([N:29]4[CH2:28][C:27]([CH3:33])([CH3:26])[O:31][C:30]4=[O:32])=[CH:3][C:4]=3[F:25])=[O:9])[CH2:11][CH2:12]2)=[N:17][CH:18]=[C:19]([CH3:24])[CH:20]=1)[CH3:23]

Participants

3

Reactant 2

HCID 1368922-Oxazolidinone, 5,5-dimethyl-HCID 58484506HCID 58484506, compound

Product 1

HCID 58484544HCID 58484544, compoundYield 49.1%

Procedure

By reaction and treatment in the same manner as in Example 1 and using (4-bromo-2-fluorophenyl)[4-(3-ethyl-5-methylpyridin-2-yl)piperazin-1-yl]methanone (539 mg) described in Preparation Example 104 and 5,5-dimethyloxazolidin-2-one (276 mg) described in Preparation Example 43, the title compound (287 mg) was obtained.

Workup

  1. customBy reaction and treatment in the same manner as in Example 1
  2. customdescribed in Preparation Example 43

Sources & evidence

ORD record
ord-79ad3831ba3f421cb069bb15df00b72f
Source dataset
uspto-grants-2013_01
Patent number
US08354401B2

Reaction notes

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