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Potassium Carbonate → (E)-ethyl 3-(4-chloro-1H-pyrrolo[2,3-b]pyridin-5-yl)acrylate

HRID 1944602
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HRID 1944602 반응식
[Cl:1][C:2]1[C:7]([CH:8]=O)=[CH:6][N:5]=[C:4]2[N:10]([Si](C(C)C)(C(C)C)C(C)C)[CH:11]=[CH:12][C:3]=12.C([O-])([O-])=[O:24].[K+].[K+].[O:29]1[CH2:34][CH2:33]O[CH2:31][CH2:30]1>CCOC(C)=O>[Cl:1][C:2]1[C:7](/[CH:8]=[CH:31]/[C:30]([O:29][CH2:34][CH3:33])=[O:24])=[CH:6][N:5]=[C:4]2[NH:10][CH:11]=[CH:12][C:3]=12
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참가 물질

5

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HCID 11430Potassium CarbonateHCID 312751,4-DioxaneHCID 497590451H-Pyrrolo[2,3-B]pyridine-5-carboxaldehyde, 4-chloro-1-[tris(1-methylethyl)silyl]-

생성물 1

HCID 58524967(E)-ethyl 3-(4-chloro-1H-pyrrolo[2,3-b]pyridin-5-yl)acrylate수율 50%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
80 °C

실험 절차

To a solution of compound 4.0 4-chloro-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde (1.7 g, 5 mmol, 1 equiv.) in dioxane (20 mL) at room temperature was added triethyl phosphonoacetate (3 mL, 15 mmol, 3 equiv.) and K2CO3 (3.45 g, 25 mmol, 5 equiv.). The resulting mixture was heated overnight at 80° C. under argon. Upon cooling to room temperature, the mixture was diluted with EtOAc (50 mL) and washed with water (50 mL) and brine (50 mL). The organic phase was dried over Na2SO4, after removal of solvent under vacuum. The resulting residue was purified with flash chromatography (Hexanes: EtOAc=6:1) to afford the desired product 4.1 (E)-ethyl 3-(4-chloro-1H-pyrrolo[2,3-b]pyridin-5-yl)acrylate (0.63 g; 50%). LC-MS: (M+H) 251.29

후처리

  1. temperatureUpon cooling to room temperature
  2. washwashed with water (50 mL) and brine (50 mL)
  3. dry with materialThe organic phase was dried over Na2SO4
  4. customafter removal of solvent under vacuum
  5. customThe resulting residue was purified with flash chromatography (Hexanes: EtOAc=6:1)

출처 및 근거

ORD 기록
ord-b4a449153b8245ecbafd72c5fa02982e
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08394818B2

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