Hydrochloric Acid → Dipyridin-3-ylmethanol

HRID 1186399노트

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HRID 1186399 반응식
C([Li])CCC.CCCCCC.Br[C:13]1[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=1.[CH:19](=[O:26])[C:20]1[CH:25]=[CH:24][CH:23]=[N:22][CH:21]=1.Cl>C(OCC)(=O)C.O1CCCC1.C1(C)C=CC=CC=1>[N:15]1[CH:16]=[CH:17][CH:18]=[C:13]([CH:19]([C:20]2[CH:21]=[N:22][CH:23]=[CH:24][CH:25]=2)[OH:26])[CH:14]=1

참가 물질

9

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온도
-60 °C

실험 절차

A 1.55 mol/L solution of n-butyllithium in hexane (2.24 mL, 3.48 mmol) was added to toluene (6 mL) and the mixture was cooled to −60° C. under a nitrogen atmosphere. To this, a toluene solution (2 mL) of 3-bromopyridine (500 mg, 3.16 mmol) was added dropwise and the mixture was stirred for 30 minutes. Tetrahydrofuran (2 mL) and nicotinaldehyde (0.358 mL, 3.79 mmol) were added to the reaction mixture and the mixture was stirred at a temperature of −60° C. to −15° C. for 30 minutes. After 4 mol/L hydrochloric acid (2.37 mL, 9.48 mmol) was added to the reaction mixture, extraction with ethyl acetate was performed, followed by washing with saturated sodium bicarbonate and brine, and drying over anhydrous sodium sulfate. The solvent was evaporated off under reduced pressure, and the residue was purified by preparative thin-layer chromatography (chloroform/methanol=12/1) to give dipyridin-3-ylmethanol (Compound EP) (235 mg, yield: 40%).

후처리

  1. stirringthe mixture was stirred at a temperature of −60° C. to −15° C. for 30 minutes
  2. washby washing with saturated sodium bicarbonate and brine
  3. dry with materialdrying over anhydrous sodium sulfate
  4. customThe solvent was evaporated off under reduced pressure
  5. customthe residue was purified by preparative thin-layer chromatography (chloroform/methanol=12/1)

출처 및 근거

ORD 기록
ord-b72fcd15d42248db8ec68c1227474b96
출처 데이터셋
uspto-grants-2014_03
특허 번호
US08673908B2

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