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Diethyl Oxalate → Ethyl(3-fluoro-2-iodopyridin-4-yl)oxoacetate

HRID 895156
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인쇄 미리보기

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HRID 895156 반응식
C([Li])CCC.C(N[CH:10]([CH3:12])[CH3:11])(C)C.[F:13][C:14]1C=NC=C[C:19]=1[I:20].[C:21]([O:28][CH2:29][CH3:30])(=[O:27])[C:22]([O:24]CC)=O.[Cl-].[NH4+:32]>O1CCCC1>[F:13][C:14]1[C:19]([I:20])=[N:32][CH:12]=[CH:10][C:11]=1[C:22](=[O:24])[C:21]([O:28][CH2:29][CH3:30])=[O:27]
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참가 물질

7

반응물 5

HCID 7268Diethyl OxalateHCID 7912DiisopropylamineHCID 25517Ammonium ChlorideHCID 109986363-Fluoro-4-IodopyridineHCID 178418339Butyllithium

생성물 1

HCID 86600101Ethyl(3-fluoro-2-iodopyridin-4-yl)oxoacetate

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매
3회

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온도
0 °C

실험 절차

n-Butyllithium (1.59M in hexane) (1.75 ml, 2.78 mmol) was added to a solution of diisopropylamine (390 μl, 2.78 mmol) in tetrahydrofuran (10 ml) at −78° C., and the mixture was warmed up to 0° C., then stirred for 30 minutes. The mixture was again cooled down to −78° C. A solution of 3-fluoro-4-iodopyridine (500 mg, 2.24 mmol) synthesized by the method of P. Rocca et. al. (Tetrahedron 49,49-64(1993)) in tetrahydrofuran (4 ml) was added to said mixture, and the resulting mixture was stirred for 1.5 hours. The reaction mixture was dropwise added to a solution of diethyl oxalate (900 μl, 6.63 mmol) in tetrahydrofuran (10 ml) at −78° C. under stirring. The mixture was warmed up to room temperature and stirred for 20 minutes. Aqueous ammonium chloride was added to the reaction mixture, and the mixture was extracted with chloroform. The extract was dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane:ethyl acetate, 3:2) to give the title compound (659 mg).

후처리

  1. temperatureThe mixture was again cooled down to −78° C
  2. stirringthe resulting mixture was stirred for 1.5 hours
  3. stirringunder stirring
  4. temperatureThe mixture was warmed up to room temperature
  5. stirringstirred for 20 minutes
  6. extractionthe mixture was extracted with chloroform
  7. dry with materialThe extract was dried over anhydrous magnesium sulfate
  8. concentrationconcentrated in vacuo
  9. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate, 3:2)

출처 및 근거

ORD 기록
ord-7be70e677c5a4bd2b6be9e2418aa1892
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06914062B2

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