3-Pyridinecarboxaldehyde → 2-Methoxy-5-(pyrid-3-ylhydroxymethyl)pyridine

HRID 1607030

반응식

HRID 1607030 반응식
Br[C:2]1[CH:3]=[CH:4][C:5]([O:8][CH3:9])=[N:6][CH:7]=1.C([Li])CCC.[N:15]1[CH:20]=[CH:19][CH:18]=[C:17]([CH:21]=[O:22])[CH:16]=1.[Cl-].[NH4+]>CCCCCC.CCOCC.O>[CH3:9][O:8][C:5]1[CH:4]=[CH:3][C:2]([CH:21]([C:17]2[CH:16]=[N:15][CH:20]=[CH:19][CH:18]=2)[OH:22])=[CH:7][N:6]=1

참가 물질

8

반응 조건

온도
-50 °C

실험 절차

5-Bromo-2-methoxypyridine (188 g) was added over 30 minutes to a 1.55 molar solution of n-butyllithium in hexane (770 ml) and ether (1200 ml) stirred at -50° C. The suspension was stirred for 1 hour when pyridine-3-carboxaldehyde (112 g) in ether (200 ml) was added over 30 minutes. The solution was stirred for 3.5 hr and then allowed to warm to ambient temperature. Saturated ammonium chloride solution (100 ml) and water (2 L) was added and the solution was concentrated to ca. 2.5 L in vacuo. Chloroform (3 L) was added and the title compound (41.3 g) was collected by filtration. The chloroform layer was separated, dried over magnesium sulphate and the solvent was removed under reduced pressure. The residue was treated with chloroform (200 ml) and filtered to give a second crop of the product (51.01 g). Recrystallisation from isopropanol/ether gave the title compound, m.p. 129°-130° C.

후처리

  1. additionwas added over 30 minutes
  2. stirringThe solution was stirred for 3.5 hr
  3. temperatureto warm to ambient temperature
  4. concentrationthe solution was concentrated to ca. 2.5 L in vacuo
  5. additionChloroform (3 L) was added
  6. filtrationthe title compound (41.3 g) was collected by filtration
  7. customThe chloroform layer was separated
  8. dry with materialdried over magnesium sulphate
  9. customthe solvent was removed under reduced pressure
  10. additionThe residue was treated with chloroform (200 ml)
  11. filtrationfiltered

출처 및 근거

ORD 기록
ord-4388444417d44b2c8a5325320d9e711b
출처 데이터셋
uspto-grants-1989_09
특허 번호
US04863933

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