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Isopropanol → HCID 13374342, 화합물

HRID 2291114
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HRID 2291114 반응식
[Na].[Cl:2][C:3]1[N:8]=[C:7](Cl)[C:6]([CH2:10][C:11]2[CH:12]=[N:13][C:14]([CH3:17])=[CH:15][CH:16]=2)=[CH:5][N:4]=1.[CH:18]([OH:21])([CH3:20])[CH3:19]>>[Cl:2][C:3]1[N:8]=[C:7]([O:21][CH:18]([CH3:20])[CH3:19])[C:6]([CH2:10][C:11]2[CH:12]=[N:13][C:14]([CH3:17])=[CH:15][CH:16]=2)=[CH:5][N:4]=1
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참가 물질

4

반응물 3

HCID 3776Isopropanol2회HCID 5360545SodiumHCID 133743332,4-Dichloro-5-[(6-methyl-3-pyridinyl)methyl]pyrimidine

생성물 1

HCID 13374342HCID 13374342, 화합물수율 87%

실험 절차

A solution of 1.38 g (0.06 g-atom) of sodium metal in 25 ml of isopropanol was heated to reflux until complete dissolution of the metal. The alkoxide solution was cooled to -10° and treated dropwise with a solution of 15.0 g (60 mmol) of 2,4-dichloro-5-[(6-methyl-3-pyridinyl)methyl]pyrimidine prepared as in Example 1 in 60 ml of isopropanol. The resulting mixture was allowed to warm to room temperature over 18 hours and was then concentrated. The resulting oil was dissolved in ethyl acetate, filtered, washed with water, dried over magnesium sulfate, filtered, concentrated and dried under vacuum to give 14.5 g (0.052 mol, 87%) of 2-chloro-4-isopropoxy-5-[(6-methyl-3-pyridinyl)methyl]pyrimidine. Recrystallization from ethyl acetate and petroleum ether gave yellow crystals: m.p. 38°-42°.

후처리

  1. temperatureto reflux until complete dissolution of the metal
  2. concentrationwas then concentrated
  3. dissolutionThe resulting oil was dissolved in ethyl acetate
  4. filtrationfiltered
  5. washwashed with water
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customdried under vacuum

출처 및 근거

ORD 기록
ord-432dad72ae964bee9077476cbff7db39
출처 데이터셋
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04620001

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