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Potassium Carbonate → (2S,4S)-4-fluoro-1-(2-((2-methyl-4-oxo-4-pyrrolidin-1-ylbutan-2-yl)amino)acetyl)pyrrolidine-2-carbonitrile

HRID 910402
ノート
印刷プレビュー

反応式

HRID 910402 の反応式
FC(F)(F)C(O)=O.[NH2:8][C:9]([CH3:19])([CH3:18])[CH2:10][C:11]([N:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1)=[O:12].C(=O)([O-])[O-].[K+].[K+].Br[CH2:27][C:28]([N:30]1[CH2:34][C@@H:33]([F:35])[CH2:32][C@H:31]1[C:36]#[N:37])=[O:29]>C1COCC1>[CH3:18][C:9]([NH:8][CH2:27][C:28]([N:30]1[CH2:34][C@@H:33]([F:35])[CH2:32][C@H:31]1[C:36]#[N:37])=[O:29])([CH3:19])[CH2:10][C:11](=[O:12])[N:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1
参加物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 21090395(2S,4S)-1-(2-bromoacetyl)-4-fluoropyrrolidine-2-carbonitrileHCID 673922513-amino-3-methyl-1-(1-pyrrolidinyl)-1-Butanone 2,2,2-trifluoroacetate

生成物 1

HCID 44201003(2S,4S)-4-fluoro-1-(2-((2-methyl-4-oxo-4-pyrrolidin-1-ylbutan-2-yl)amino)acetyl)pyrrolidine-2-carbonitrile収率 74%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

実験手順

To a stirred solution of 3-amino-3-methyl-1-pyrrolidin-1-yl-butan-1-one trifluoroacetic acid (0.28 g, 1 mmol) in anhydrous THF (5 mL) was added potassium carbonate (0.55 g, 4 mmol). After stirred at room temperature for 1 h, the mixture was filtered through a Celite pad, and rinsed with ethyl acetate (5 mL). To the above filtrate was added (2S,4S)-1-(2-bromoacetyl)-4-fluoropyrrolidine-2-carbonitrile (0.12 g, 0.5 mmol) and the reaction mixture was stirred at room temperature under nitrogen for 12 h. Most of solvent was removed under reduced pressure and the residue was partitioned between CH2Cl2 (20 mL) and H2O (5 mL). The aqueous layer was further extracted with CH2Cl2 (10 mL). The combined organic layers were dried over magnesium sulfate, filtered, and concentrated under reduced pressure to yield a crude viscous oil. The crude oil was purified by chromatography (silica gel, 4 to 10% CH3OH/CH2Cl2 gradient) to give compound 1 (0.12 g, 74% overall yield) as a white solid.

後処理

  1. filtrationthe mixture was filtered through a Celite pad
  2. washrinsed with ethyl acetate (5 mL)
  3. stirringthe reaction mixture was stirred at room temperature under nitrogen for 12 h
  4. customMost of solvent was removed under reduced pressure
  5. customthe residue was partitioned between CH2Cl2 (20 mL) and H2O (5 mL)
  6. extractionThe aqueous layer was further extracted with CH2Cl2 (10 mL)
  7. dry with materialThe combined organic layers were dried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customto yield a crude viscous oil
  11. customThe crude oil was purified by chromatography (silica gel, 4 to 10% CH3OH/CH2Cl2 gradient)

出典と根拠

ORDレコード
ord-75b4ec1324a3404eb072a3ae293c6661
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08022096B2

反応ノート

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