反应 #1973923

ord-51dba3c42d9742caa5f52dc5cdc9f010

反应方程式

CC(O)c1ccc(N)cc1
p-aminophenylethanol
CCN(CC)CC
triethyl amine
C#CCCC(=O)O.O=C1CCC(=O)N1O
N-hydroxysuccinimide-(4-pentynoate)
C#CCCC(=O)Nc1ccc(CCO)cc1
N-(4-(2-(Hydroxy)Ethyl)Phenyl)Pent-4-Ynamide

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The crude reaction product
  2. 2
    浓缩was concentrated
  3. 3
    workup.DISSOLUTIONdissolved in 10 mL of ethyl acetate
  4. 4
    洗涤washed with 5 mL of water
  5. 5
    干燥The organic phase was dried with MgSO4
  6. 6
    过滤filtered
  7. 7
    其他the solvent was evaporated
  8. 8
    其他The product was further purified by column chromatography on silica gel eluting with a gradient of toluene (T) and ethyl acetate (E) from 4:1 to 1:2 (T:E)

实验过程

N-hydroxysuccinimide-(4-pentynoate) (Ref: Malkoch, M.; Schleicher, K.; Drockenmuller, E.; Hawker, C. J.; Russell, T. P.; Wu, P.; Fokin, V. V., Structurally Diverse Dendritic Libraries: A Highly Efficient Functionalization Approach Using Click Chemistry. Macromolecules 2005, 38, (9), 3663-3678.) (200 mg, 1.0 mmol) and p-aminophenylethanol (125 mg, 0.9 mmol) were dissolved in 2 mL of dichloromethane together with triethyl amine (140 μL, 1.0 mmol), and 5 drops of dimethyl formamide. The reaction mixture was stirred at room temperature for 2 hours. The crude reaction product was concentrated, dissolved in 10 mL of ethyl acetate and washed with 5 mL of water followed by, 5 mL of 0.5 M HCl (aq.), 5 mL of 10 NaHCO3 (aq.) and finally 5 mL of water. The organic phase was dried with MgSO4, filtered, and the solvent was evaporated. The product was further purified by column chromatography on silica gel eluting with a gradient of toluene (T) and ethyl acetate (E) from 4:1 to 1:2 (T:E). The product N-(4-(2-(hydroxy)ethyl)phenyl)pent-4-ynamide was characterized by NMR and MALDI-TOF.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08501212B2uspto-grants-2013_08