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Potassium Phosphate, Tribasic → 4-Cyclopropylpyridine-2-carbonitrile

HRID 931124
ノート
印刷プレビュー

反応式

HRID 931124 の反応式
Br[C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C:8]#[N:9])[CH:3]=1.[CH:10]1(B(O)O)[CH2:12][CH2:11]1.[O-]P([O-])([O-])=O.[K+].[K+].[K+]>O1CCCC1>[CH:10]1([C:2]2[CH:7]=[CH:6][N:5]=[C:4]([C:8]#[N:9])[CH:3]=2)[CH2:12][CH2:11]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 62657Potassium Phosphate, TribasicHCID 6932834-Bromo-2-cyanopyridineHCID 2760897Cyclopropylboronic acid

生成物 1

HCID 753556264-Cyclopropylpyridine-2-carbonitrile収率 70%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 4-bromopicolinonitrile (0.2 g, 1.1 mmol) in tetrahydrofuran were added cyclopropyl boronic acid (0.093 g, 1.1 mmol), and potassium phosphate tribasic (0.694 g, 3.2 mmol). The resulting reaction mixture was degassed with nitrogen for 10 minutes and then added Pd(OAc)2 and S-phos were added. The reaction mixture was heated at reflux for 16 h, then was diluted with water and extracted with ethyl acetate. The organic layer was concentrated under reduced pressure and the residue was purified via flash chromatography (10% ethyl acetate in petroleum ether) to afford 4-cyclopropylpicolinonitrile (0.1 g, 70%). MS (ES+APCI) (M+H) 145.2; LCMS retention time 3.02 min (Method J).

後処理

  1. customThe resulting reaction mixture
  2. customwas degassed with nitrogen for 10 minutes
  3. additionadded Pd(OAc)2 and S-phos were added
  4. temperatureThe reaction mixture was heated
  5. temperatureat reflux for 16 h
  6. additionwas diluted with water
  7. extractionextracted with ethyl acetate
  8. concentrationThe organic layer was concentrated under reduced pressure
  9. customthe residue was purified via flash chromatography (10% ethyl acetate in petroleum ether)

出典と根拠

ORDレコード
ord-b1f529bf285e495ba1537981c9778d6f
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09296745B2

反応ノート

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