반응 #2199173

ord-13acd9a2856e486e95d3b6683b2e8262

반응 방정식

CCN(C(C)C)C(C)C
DIPEA
CCCCCCNCc1ccccc1
N-Hexylbenzylamine
COc1cc(CC(=O)O)ccc1O
Homovanillic acid
CN(C)C(On1nnc2ccccc21)=[N+](C)C.F[B-](F)(F)F
TBTU
CCCCCCN(Cc1ccccc1)C(=O)Cc1ccc(O)c(OC)c1
desired product
수율 74.3%
CCCCCCN(Cc1ccccc1)C(=O)Cc1ccc(O)c(OC)c1
N-Benzyl-N-hexyl-2-(4-hydroxy-3-methoxyphenyl)acetamide
수율 74.3%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was cooled in an ice-bath
  2. 2
    기타evaporated
  3. 3
    workup.ADDITIONSodium hydrogencarbonate aqueous solution (sat.) was added into the residue
  4. 4
    추출The mixture was then extracted with ethyl acetate (×2)
  5. 5
    세척washed with water and brine
  6. 6
    건조dried (magnesium sulphate)
  7. 7
    기타evaporated

실험 절차

Homovanillic acid (182 mg, 0.999 mmol) dissolved in DMF (3 ml) was cooled in an ice-bath. N-Hexylbenzylamine (201 mg, 1.049 mmol) was added and then TBTU (337 mg, 1.049 mmol) followed by DIPEA (407 mg, 3.147 mmol). The mixture was stirred at room temperature overnight and evaporated. Sodium hydrogencarbonate aqueous solution (sat.) was added into the residue. The mixture was then extracted with ethyl acetate (×2). The extracts were combined and washed with water and brine and dried (magnesium sulphate) and evaporated. Chromatography of the residue on a column (ISOLUTE® SI, 5 g/15 ml) using DCM and then MeOH/DCM (1:99) as eluant gave 264 mg the desired product, yield 74%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07521461B2uspto-grants-2009_04