Hydrochloric Acid → (4-Chloro-6-((1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)methoxy)-1-benzothiophen-3-yl)acetic acid

HRID 591417노트

반응식

HRID 591417 반응식
C[O:2][C:3](=[O:27])[CH2:4][C:5]1[C:9]2[C:10]([Cl:26])=[CH:11][C:12]([O:14][CH2:15][C:16]3[N:20]([CH3:21])[N:19]=[C:18]([C:22]([F:25])([F:24])[F:23])[CH:17]=3)=[CH:13][C:8]=2[S:7][CH:6]=1.[OH-].[Na+].C1COCC1.Cl>O.CO>[Cl:26][C:10]1[C:9]2[C:5]([CH2:4][C:3]([OH:27])=[O:2])=[CH:6][S:7][C:8]=2[CH:13]=[C:12]([O:14][CH2:15][C:16]2[N:20]([CH3:21])[N:19]=[C:18]([C:22]([F:24])([F:23])[F:25])[CH:17]=2)[CH:11]=1

참가 물질

7

실험 절차

A mixture of methyl(4-chloro-6-((1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)methoxy)-1-benzothiophen-3-yl)acetate (1.9 g), 1N NaOH (10 mL), THF (10 mL) and MeOH (10 mL) was stirred at room temperature for 4 h. To the mixture were added 1N HCl (10 mL) and water, and the mixture was extracted with EtOAc. The organic layer was separated, washed with brine, dried over MgSO4 and concentrated in vacuo. The residual solid was washed with hexane to give the crystals (1.75 g). The crystals were recrystallized from acetone-heptane to give the title compound.

후처리

  1. extractionthe mixture was extracted with EtOAc
  2. customThe organic layer was separated
  3. washwashed with brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated in vacuo
  6. washThe residual solid was washed with hexane

출처 및 근거

ORD 기록
ord-b87264a573a24db8a83de5e6fd60a9d9
출처 데이터셋
uspto-grants-2016_01
특허 번호
US09238639B2

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