反応 #1637

ord-c88884b2244548bda021d31a20f133fd

反応方程式

Oc1ccc(CCNC[C@H](O)COc2ccc(OCc3ccccc3)cc2)cc1
(S)-1-(4-benzyloxyphenoxy)-3-[N-2-(4-hydroxyphenyl)ethylamino]propan-2-ol
BrCc1ccccc1
benzyl bromide
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
Oc1ccc(CCN(Cc2ccccc2)C[C@H](O)COc2ccc(OCc3ccccc3)cc2)cc1
title compound
Oc1ccc(CCN(Cc2ccccc2)C[C@H](O)COc2ccc(OCc3ccccc3)cc2)cc1
(S)-N-Benzyl-1(4-benzyloxyphenoxy)-3-[N-2-(4-hydroxyphenyl)ethylamino]propan-2-ol

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The mixture was filtered
  2. 2
    洗浄the residue was washed with ethyl acetate
  3. 3
    洗浄washed with water and brine
  4. 4
    その他dried
  5. 5
    その他evaporated
  6. 6
    その他Purification of the residue by flash chromatography (silica gel, 50% ethyl acetate in hexane)

実験手順

A solution of (S)-1-(4-benzyloxyphenoxy)-3-[N-2-(4-hydroxyphenyl)ethylamino]propan-2-ol (1.9 g, 4.8 mMol) and benzyl bromide (0.57 ml, 4.8 mMol) in dimethylformamide (10 ml) containing sodium carbonate (770 mg, 7.2 mMol) was stirred at room temperature for 18 hours. The mixture was filtered and the residue was washed with ethyl acetate. The filtrates were combined, washed with water and brine, dried and evaporated. Purification of the residue by flash chromatography (silica gel, 50% ethyl acetate in hexane) gave the title compound.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05726165uspto-grants-1998_03