Water → N-((2'-Cyano(1,1'-biphenyl)-4-yl)methyl)-L-valine methyl ester

HRID 875173ノート

反応式

HRID 875173 の反応式
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15]#[N:16])=[CH:5][CH:4]=1.C(=O)([O-])[O-].[K+].[K+].O.Cl.[CH3:25][O:26][C:27](=[O:33])[C@H:28]([CH:30]([CH3:32])[CH3:31])[NH2:29]>C(OCC)(=O)C>[CH3:25][O:26][C:27](=[O:33])[C@H:28]([CH:30]([CH3:32])[CH3:31])[NH:29][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15]#[N:16])=[CH:5][CH:4]=1

参加物

6

反応条件

温度
45 °C

実験手順

4′-Bromomethyl-2-cyanobiphenyl (75 g, 0.2757 moles) was added to a mixture of potassium carbonate (95.12 g), DM water (225 ml), ethyl acetate (450 ml) and L-valine methyl ester hydrochloride (55.45 g, 0.330 moles) at 20-30° C. The reaction mixture was heated to 40-50° C. and stirred for 25 h. After completion of the reaction, the ethyl acetate layer was separated at 20-30° C., added DM water (375 ml) and adjusted the pH to 0.8-1.0 with dilute hydrochloric acid at 20-30° C. The aqueous layer was separated and extracted the product in to toluene (430 ml) by adjusting the pH to 8.0-8.5 with 20% w/w aqueous sodium carbonate solution. The toluene layer was washed with DM water (225 ml), concentrated under reduced pressure and dissolved in toluene (450 ml)

後処理

  1. customAfter completion of the reaction
  2. customthe ethyl acetate layer was separated at 20-30° C.
  3. additionadded DM water (375 ml)
  4. customat 20-30° C
  5. customThe aqueous layer was separated
  6. extractionextracted the product in to toluene (430 ml)
  7. washThe toluene layer was washed with DM water (225 ml)
  8. concentrationconcentrated under reduced pressure
  9. dissolutiondissolved in toluene (450 ml)

出典と根拠

ORDレコード
ord-f80b27b44c134ce4b608391932b4f6e2
出典データセット
uspto-grants-2015_03
特許番号
US08981109B2

反応ノート

読み込み中…