反应 #1810817

ord-1630c55dfdd94748a5fcb4107ad4c87d

反应方程式

O=C(Cl)c1cc([N+](=O)[O-])ccc1N1CCOCC1
2-morpholin-4-yl-5-nitro-benzoyl chloride
C1=C(c2ccccc2)CCNC1
4-phenyl-1,2,3,6-tetrahydro-pyridine
CCN(CC)CC
NEt3
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CC=C(c2ccccc2)CC1
(2-Morpholin-4-yl-5-nitro-phenyl)-(4-phenyl-3,6-dihydro-2H-pyridin-1-yl)-methanone

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他After evaporation of the volatiles the residue
  2. 2
    其他subjected to preparative HPLC purification on reversed phase
  3. 3
    洗涤eluting with an acetonitrile/water gradient
  4. 4
    其他to yield
  5. 5
    其他after evaporation the title compound

实验过程

A mixture of 40.6 mg (0.15 mmol) of 2-morpholin-4-yl-5-nitro-benzoyl chloride, 29 mg (0.18 mmol) 4-phenyl-1,2,3,6-tetrahydro-pyridine (commercial) and 62.5 ul (0.45 mmol) NEt3 in 1 ml DCM was stirred at room temperature for 16 h. After evaporation of the volatiles the residue was taken up in 1 ml CH3CN/DMF/HCOOH 3/5/2 and subjected to preparative HPLC purification on reversed phase eluting with an acetonitrile/water gradient to yield after evaporation the title compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07485637B2uspto-grants-2009_02