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Sodium Methoxide → HCID 86662981, 화합물

HRID 71201
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HRID 71201 반응식
Cl[C:2]1[C:7]([C:8]2[O:12][C:11]([CH3:13])=[N:10][CH:9]=2)=[CH:6][CH:5]=[C:4]([Cl:14])[N:3]=1.[CH3:15][O-:16].[Na+]>CO>[Cl:14][C:4]1[N:3]=[C:2]([O:16][CH3:15])[C:7]([C:8]2[O:12][C:11]([CH3:13])=[N:10][CH:9]=2)=[CH:6][CH:5]=1
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참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 866629825-(2,6-Dichloro-3-pyridyl)-2-methyloxazole

생성물 1

HCID 86662981HCID 86662981, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a mixture of 2,6-dichloro-3-(2-methyl-1,3-oxazol-5-yl)pyridine (2.22 g) in methanol (25 mL) was added sodium methoxide (5M methanol solution, 1.9 mL) at room temperature, and the mixture was stirred under a nitrogen atmosphere over the weekend. The reaction mixture was concentrated and diluted with water, and the mixture was extracted with ethyl acetate. The organic layer was separated, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane), and separated by HPLC (column: Chiralpak AD, mobile phase: hexane/2-propanol) to give the title compound (867 mg).

후처리

  1. concentrationThe reaction mixture was concentrated
  2. additiondiluted with water
  3. extractionthe mixture was extracted with ethyl acetate
  4. customThe organic layer was separated
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was evaporated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (ethyl acetate/hexane)
  8. customseparated by HPLC (column: Chiralpak AD, mobile phase: hexane/2-propanol)

출처 및 근거

ORD 기록
ord-ae881f1640b14f06ab1590c6efe626cc
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822699B2

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