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Sodium Hydroxide → 6-[(Tetrahydro-2H-pyran-4-yl)oxy]-3-pyridinecarboxylic acid

HRID 341541
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HRID 341541 반응식
[O:1]1[CH2:6][CH2:5][CH:4]([O:7][C:8]2[N:13]=[CH:12][C:11]([C:14]([O:16]CC)=[O:15])=[CH:10][CH:9]=2)[CH2:3][CH2:2]1.[OH-].[Na+]>CCO>[O:1]1[CH2:2][CH2:3][CH:4]([O:7][C:8]2[N:13]=[CH:12][C:11]([C:14]([OH:16])=[O:15])=[CH:10][CH:9]=2)[CH2:5][CH2:6]1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 66803133HCID 66803133, 화합물2회

생성물 1

HCID 242295766-[(Tetrahydro-2H-pyran-4-yl)oxy]-3-pyridinecarboxylic acid수율 76.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Ethyl 6-(oxan-4-yloxy)pyridine-3-carboxylate (Intermediate 236, 0.239 g, 0.95 mmol) was dissolved in EtOH (5 mL), 2M aq. sodium hydroxide (1.43 mL, 2.85 mmol) was added and the mixture was stirred at room temperature for 4 h. The mixture was concentrated under vacuum and the residue acidified to pH 6 by adding 2M aq. hydrochloric acid. The mixture was then extracted with DCM, followed by chloroform/isopropanol. The organic layer was separated using a hydrophobic frit and concentrated under vacuum to afford the title compound as a white solid (0.162 g, 47%), which was used directly in the next step without further purification. Method C HPLC-MS: MH+ requires m/z=224 Found: m/z=224, Rt=1.06 min (91%).

후처리

  1. concentrationThe mixture was concentrated under vacuum
  2. additionby adding 2M aq. hydrochloric acid
  3. extractionThe mixture was then extracted with DCM
  4. customThe organic layer was separated
  5. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-c3670c1bf63e4ed59c92ed74235a0c4c
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895733B2

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