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2-Fluoro-3-(1,4-dioxaspiro[4.5]decan-8-YL)pyrazine → 4-(3-Fluoropyrazin-2-yl)cyclohexanone

HRID 454900
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HRID 454900 반응식
[F:1][C:2]1[C:7]([CH:8]2[CH2:17][CH2:16][C:11]3(OCC[O:12]3)[CH2:10][CH2:9]2)=[N:6][CH:5]=[CH:4][N:3]=1>Cl.CC(C)=O>[F:1][C:2]1[C:7]([CH:8]2[CH2:9][CH2:10][C:11](=[O:12])[CH2:16][CH2:17]2)=[N:6][CH:5]=[CH:4][N:3]=1
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참가 물질

4

반응물 1

HCID 585479812-Fluoro-3-(1,4-dioxaspiro[4.5]decan-8-YL)pyrazine

생성물 1

HCID 585477714-(3-Fluoropyrazin-2-yl)cyclohexanone수율 70.1%

시약·촉매·용매 2

HCID 180Acetone용매2회HCID 313Hydrochloric Acid용매

실험 절차

A solution of 2-fluoro-3-(1,4-dioxaspiro[4.5]decan-8-yl)pyrazine (91 g, 0.382 mol, 1.0 eq.) in 1N aqueous HCl (573 mL) and acetone (4 L) was heated to 37° C. overnight. The reaction mixture was cooled to room temperature and most of acetone was removed under reduced pressure. The crude material was diluted with EtOAc (4 L) and the solution was washed with aqueous saturated NaHCO3 (500 mL×2), water (500 mL), brine (500 mL), dried over Na2SO4, filtered, and evaporated. The crude product was purified by column chromatography (100% hexanes to 50% EtOAc in hexanes, Rf=0.3 in 30% EtOAc in hexanes) to give 52 g (70% yield) of 4-(3-fluoropyrazin-2-yl)cyclohexanone. GC-MS: 195 (M+1); calcd for C10H11FN2O: 194.21

후처리

  1. customwas removed under reduced pressure
  2. additionThe crude material was diluted with EtOAc (4 L)
  3. washthe solution was washed with aqueous saturated NaHCO3 (500 mL×2), water (500 mL), brine (500 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude product was purified by column chromatography (100% hexanes to 50% EtOAc in hexanes, Rf=0.3 in 30% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-9fd34bc2fff14cdfae81c288b7f37daf
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08497265B2

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