反応 #577240

ord-3686e9d92cd049048910744240f2e15e

反応方程式

Cl
HCl
CCCCCCCCc1ccc(CCC(N)(CO)COP(=O)(O)O)cc1
(R/S)-FTY720-phosphate
CCCCCCCCc1ccc(CCC(N)(CO)COP(=O)(O)O)cc1
Phosphoric acid mono-[(R/S)-2-amino-2-hydroxymethyl-4-(4-octyl-phenyl)-butyl]ester
O=C(O)CN(CCN(CC(=O)O)CC(=O)O)CC(=O)O
EDTA
OB(O)O
boric acid
CCCCCCCCc1ccc(CCC(CO)(COP(=O)(O)O)N2Cc3ccccc3C2=O)cc1
Phosphoric acid mono-[(R/S)-2-hydroxymethyl-4-(4-octyl-phenyl)-2-(1-oxo-1,3-dihydro-isoindol-2-yl)-butyl]ester

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONAfter addition of OPA (33 mg, 0.25 mmol)
  2. 2
    抽出extracted with ethylacetate (three times)
  3. 3
    乾燥The organic layer is dried over Na2SO4
  4. 4
    その他the compound is purified on silica gel

実験手順

The endproduct of step d) ((R/S)-FTY720-phosphate) (50 mg; 0.125 mmol) is suspended in a solution of EDTA (0.5 ml; 10 mM in water) and aqueous boric acid (0.5 ml; 3% in water; adjusted to pH 10.5 with aqueous KOH10%). After addition of OPA (33 mg, 0.25 mmol), dissolved in ethanol (0.5 ml), the reaction is kept at RT for 1 hour (ultrasound). After that the pH is adjusted to 3.5 (aqueous HCl; 1N) and extracted with ethylacetate (three times). The organic layer is dried over Na2SO4 and the compound is purified on silica gel using methylenechloride/methanol (95/5→0/100) as mobile phase.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07528120B2uspto-grants-2009_05