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Hydrochloric Acid → 3-{4-[4-(3,5-Dimethylpyridin-2-yl)piperazine-1-carbonyl]-3-(2-oxoimidazolidin-1-yl)phenyl}oxazolidin-2-one

HRID 1804288
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HRID 1804288 반응식
C([N:4]1[CH2:8][CH2:7][N:6]([C:9]2[CH:10]=[C:11]([N:31]3[CH2:35][CH2:34][O:33][C:32]3=[O:36])[CH:12]=[CH:13][C:14]=2[C:15]([N:17]2[CH2:22][CH2:21][N:20]([C:23]3[C:28]([CH3:29])=[CH:27][C:26]([CH3:30])=[CH:25][N:24]=3)[CH2:19][CH2:18]2)=[O:16])[C:5]1=[O:37])(=O)C.CO.[OH-].[Na+].Cl>O>[CH3:29][C:28]1[C:23]([N:20]2[CH2:21][CH2:22][N:17]([C:15]([C:14]3[CH:13]=[CH:12][C:11]([N:31]4[CH2:35][CH2:34][O:33][C:32]4=[O:36])=[CH:10][C:9]=3[N:6]3[CH2:7][CH2:8][NH:4][C:5]3=[O:37])=[O:16])[CH2:18][CH2:19]2)=[N:24][CH:25]=[C:26]([CH3:30])[CH:27]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 14798Sodium HydroxideHCID 673809123-{3-(3-Acetyl-2-oxoimidazolidin-1-yl)-4-[4-(3,5-dimethylpyridin-2-yl)piperazine-1-carbonyl]phenyl}oxazolidin-2-one

생성물 1

HCID 584845653-{4-[4-(3,5-Dimethylpyridin-2-yl)piperazine-1-carbonyl]-3-(2-oxoimidazolidin-1-yl)phenyl}oxazolidin-2-one수율 9.1%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
50 °C

실험 절차

To 3-{3-(3-acetyl-2-oxoimidazolidin-1-yl)-4-[4-(3,5-dimethylpyridin-2-yl)piperazine-1-carbonyl]phenyl}oxazolidin-2-one (156 mg) described in Example 209 were added methanol (2 mL) and 1N aqueous sodium hydroxide solution (0.31 mL), and the mixture was stirred at 50° C. 1N hydrochloric acid (0.31 mL) and water were added, and the mixture was extracted with ethyl acetate. The solvent was evaporated, and the residue was purified by column chromatography (ethyl acetate:methanol) to give the title compound (13 mg).

후처리

  1. extractionthe mixture was extracted with ethyl acetate
  2. customThe solvent was evaporated
  3. customthe residue was purified by column chromatography (ethyl acetate:methanol)

출처 및 근거

ORD 기록
ord-0aaf63ca98944fcb838ccf69ccfc18be
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354401B2

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