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Dicyclohexylcarbodiimide → (S)-5-(1-amino-2-methylpropyl)-3-methyl-1,2,4-oxadiazole

HRID 23761
ノート
印刷プレビュー

反応式

HRID 23761 の反応式
C([NH:8][C@H:9]([C:13]([OH:15])=O)[CH:10]([CH3:12])[CH3:11])(OC(C)(C)C)=O.C1(N=C=NC2CCCCC2)CCCCC1.[C:31](=[N:34]O)([NH2:33])[CH3:32]>ClCCl.N1C=CC=CC=1>[NH2:8][C@H:9]([C:13]1[O:15][N:34]=[C:31]([CH3:32])[N:33]=1)[CH:10]([CH3:11])[CH3:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 10868DicyclohexylcarbodiimideHCID 30926N-HydroxyacetamidineHCID 83693Boc-L-Valine

生成物 1

HCID 29550895(S)-5-(1-amino-2-methylpropyl)-3-methyl-1,2,4-oxadiazole

試薬・触媒・溶媒 2

HCID 1049Pyridine溶媒HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of BOC-L-valine (4.34 g, 20.0 mmol) in dichloromethane (20 mL) was cooled to 0° C. and treated dropwise with a solution of dicyclohexylcarbodiimide (2.06 g, 10.0 mmol) in dichloromethane (5 mL). After 1 hour the white solid which had formed was removed by filtration and the filtrate concentrated under reduced pressure. The residue was dissolved in pyridine (15 mL) and treated with acetamidoxime (488 mg, 6.6 mmol) in pyridine (5 mL) and the mixture heated at reflux for 1 hour. The pyridine was evaporated under reduced pressure and the residue partitioned between ethyl acetate and water. The organic phase was washed several times with water, dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel using 10% ethyl acetate in hexanes to elute the product (0.62 g, 25%) as a white solid.

後処理

  1. customAfter 1 hour the white solid which had formed
  2. customwas removed by filtration
  3. concentrationthe filtrate concentrated under reduced pressure
  4. dissolutionThe residue was dissolved in pyridine (15 mL)
  5. temperaturethe mixture heated
  6. temperatureat reflux for 1 hour
  7. customThe pyridine was evaporated under reduced pressure
  8. customthe residue partitioned between ethyl acetate and water
  9. washThe organic phase was washed several times with water
  10. dry with materialdried over magnesium sulfate
  11. concentrationconcentrated
  12. customThe residue was chromatographed on silica gel using 10% ethyl acetate in hexanes
  13. washto elute the product (0.62 g, 25%) as a white solid

出典と根拠

ORDレコード
ord-63c05ebf483642babd18bb6d0f623481
出典データセット
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06852745B2

反応ノート

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