反应 #434973

ord-5e3de05ac28342f89a8a676049726120

反应方程式

O=C1C(CCC(O)c2ccc(F)cc2F)C(c2ccc(OCCOCF)cc2)N1c1ccc(F)cc1F
1-(4-fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-(4-hydroxyphenyl)azetidin-2-one
O=C1C(CCC(O)c2ccc(F)cc2F)C(c2ccc(OCCOCF)cc2)N1c1ccc(F)cc1F
1-(4-fluorofluorophenyl)-3-[3-(4-fluorofluorophenyl)-3-hydroxypropyl]-4-[4-(2-fluoromethoxyethoxy)phenyl]azetidin-2-one
O=C([O-])[O-].[K+].[K+]
potassium carbonate
O=S1(=O)CCCCO1
butanesultone
O=C1C(CCC(O)c2ccc(F)cc2)C(c2ccc(OCCCCS(=O)(=O)O)cc2)N1c1ccc(F)cc1
product
O=C1C(CCC(O)c2ccc(F)cc2)C(c2ccc(OCCCCS(=O)(=O)O)cc2)N1c1ccc(F)cc1
4-(4-{1-(4-Fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]4-oxoazetidin-2-yl}phenoxy)butane-1-sulfonic acid

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤The reaction solution was filtered
  2. 2
    浓缩concentrated under oil pump vacuum
  3. 3
    其他The residue was chromatographed on a 10 g SiO2 cartridge (dichloromethane/methanol=5/1)
  4. 4
    其他crystallized from diethyl ether

实验过程

250 mg of 1-(4-fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-(4-hydroxyphenyl)azetidin-2-one (7) were dissolved in 6 ml of absolute dimethylformamide. 337 mg of powdered potassium carbonate and 69 μl of 1,4,-butanesultone were added. The mixture was stirred at room temperature overnight. The reaction solution was filtered and concentrated under oil pump vacuum. The residue was chromatographed on a 10 g SiO2 cartridge (dichloromethane/methanol=5/1) and crystallized from diethyl ether. The product (131 mg) was obtained as a solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07176193B2uspto-grants-2007_02