反応 #2199155

ord-773370379490479681c9b8724b38bbad

反応方程式

Cl
hydrochloric acid
CCCCCCNCc1ccccc1
N-hexylbenzylamine
COC(=O)c1ccccc1COc1cccc(CC(=O)O)c1
(3-{[2-(Methoxycarbonyl)benzyl]oxy}phenyl)acetic acid
ClCCCl
EDC
CCCCCCN(Cc1ccccc1)C(=O)Cc1cccc(OCc2ccccc2C(=O)OC)c1
Methyl 2-[(3-{2-[benzyl(hexyl)amino]-2-oxoethyl}phenoxy)methyl]benzoate

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The two phases were separated
  2. 2
    ろ過Filter Tube
  3. 3
    その他The obtained organic portion was evaporated in vacuum and 59 mg crude oil product
  4. 4
    workup.WAITwas left

実験手順

(3-{[2-(Methoxycarbonyl)benzyl]oxy}phenyl)acetic acid (60 mg, 0.2 mmol) was dissolved in DCM (2 ml), N-hexylbenzylamine (46 mg, 0.24 mmol) was added, then EDC (46 mg, 0.24 mmol) was added and then DMAP (29.3 mg, 0.24 mmol) was added. The mixture was stirred at room temperature overnight. 1% hydrochloric acid (1 ml) and water (1 ml) were added into the mixture. The two phases were separated by using a Whatman Filter Tube. The obtained organic portion was evaporated in vacuum and 59 mg crude oil product was left. It was then used directly in next step.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07521461B2uspto-grants-2009_04