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Water → (5R)-5-[(E)-2-(5-cyclopropyl-6-methoxypyridin-2-yl)-2-(pyridin-4-yl)ethenyl]pyrrolidin-2-one

HRID 70632
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HRID 70632 반응식
[N:1]1[CH:6]=[CH:5][C:4]([Sn](CCCC)(CCCC)CCCC)=[CH:3][CH:2]=1.O1C=CC=C1P(C1OC=CC=1)C1OC=CC=1.Br/[C:37](/[C:45]1[CH:50]=[CH:49][C:48]([CH:51]2[CH2:53][CH2:52]2)=[C:47]([O:54][CH3:55])[N:46]=1)=[CH:38]\[C@@H:39]1[NH:43][C:42](=[O:44])[CH2:41][CH2:40]1.O>O1CCOCC1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[CH:51]1([C:48]2[CH:49]=[CH:50][C:45](/[C:37](/[C:4]3[CH:3]=[CH:2][N:1]=[CH:6][CH:5]=3)=[CH:38]/[C@@H:39]3[NH:43][C:42](=[O:44])[CH2:41][CH2:40]3)=[N:46][C:47]=2[O:54][CH3:55])[CH2:52][CH2:53]1
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참가 물질

7

반응물 4

HCID 962WaterHCID 521585Tris(furan-2-yl)phosphaneHCID 27373184-(Tri-n-butylstannyl)pyridineHCID 58452792(5R)-5-[(Z)-2-bromo-2-(5-cyclopropyl-6-methoxypyridin-2-yl)ethenyl]pyrrolidin-2-one

생성물 1

HCID 67398901(5R)-5-[(E)-2-(5-cyclopropyl-6-methoxypyridin-2-yl)-2-(pyridin-4-yl)ethenyl]pyrrolidin-2-one

시약·촉매·용매 2

HCID 9811564
Bis(dibenzylideneacetone)palladium
촉매
HCID 312751,4-Dioxane용매

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온도
90 °C

실험 절차

4-Pyridyltributyltin (218 mg), tris(dibenzylideneacetone)dipalladium (27 mg) and tri(2-furyl)phosphine (42 mg) were added to a solution of (5R)-5-[(Z)-2-bromo-2-(5-cyclopropyl-6-methoxypyridin-2-yl)ethenyl]pyrrolidin-2-one obtained in Reference Example 4-24 (100 mg) in 1,4-dioxane (2 mL), and the mixture was stirred at 90° C. for four hours. The reaction solution was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was purified by NH-silica gel column chromatography (hexane:ethyl acetate=1:1→0:1) to give (5R)-5-[(E)-2-(5-cyclopropyl-6-methoxypyridin-2-yl)-2-(pyridin-4-yl)ethenyl]pyrrolidin-2-one as a colorless amorphous (42 mg).

후처리

  1. extractionfollowed by extraction with ethyl acetate
  2. washThe organic layer was washed with brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. customThe solvent was then evaporated under reduced pressure
  6. customThe residue was purified by NH-silica gel column chromatography (hexane:ethyl acetate=1:1→0:1)

출처 및 근거

ORD 기록
ord-ba9cd757a59246dd892d1e89dfc17ab1
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822503B2

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