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

HRID 1944602
ノート
印刷プレビュー

反応式

HRID 1944602 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

反応条件

温度
80 °C

実験手順

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

後処理

  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)

出典と根拠

ORDレコード
ord-b4a449153b8245ecbafd72c5fa02982e
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08394818B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート