反应 #78169

ord-68d8d685ff174f3fb8764293eccc5175

反应方程式

O=C([O-])[O-]
carbonate
O=P12OP3(=O)OP(=O)(O1)OP(=O)(O2)O3
phosphorus pentoxide
CCN(CC)CC.Cl
triethylamine hydrochloride
Nc1ccc(-c2ccccc2)cc1
4-aminobiphenyl
O=c1[nH]nc(Cc2ccncc2)c2ccccc12
4-(4-pyridylmethyl)-1(2H)-phthalazinone
c1ccc(-c2ccc(Nc3nnc(Cc4ccncc4)c4ccccc34)cc2)cc1
Title compound
c1ccc(-c2ccc(Nc3nnc(Cc4ccncc4)c4ccccc34)cc2)cc1
1-(4-Phenylanilino)-4-(4-pyridylmethyl)phthalazine

反应条件

温度
200°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度After cooling to RT
  2. 2
    workup.STIRRINGwith intensive stirring
  3. 3
    干燥The organic phase dried over sodium sulfate
  4. 4
    其他is evaporated under vacuum
  5. 5
    其他the residue purified by means of flash chromatography on silica gel with particle size 0.04-0.06 mm

实验过程

A mixture of 2.41 g (16.98 mmol) phosphorus pentoxide, 2.32 g (16.85 mmol) triethylamine hydrochloride, 3 g (17.73 mmol) 4-aminobiphenyl, and 1 g (4.21 mmol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone is stirred for 20 h at 200° C. under a nitrogen atmosphere. After cooling to RT, the hyalinocrystalline melt is distributed between a dichloromethane/methanol mixture (99:1) and a mixture of water and saturated aqueous carbonate solution on (1:1) with intensive stirring and the use of an ultrasonic bath. The organic phase dried over sodium sulfate is evaporated under vacuum and the residue purified by means of flash chromatography on silica gel with particle size 0.04-0.06 mm, using a dichloromethane/methanol mixture (49:1). Title compound is obtained after evaporation of the product-containing fractions under vacuum and recrystallization of the residue from acetonitrile; m.p. 189-191 °C.; ESI-MS: (M+H)+=389.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06710047B2uspto-grants-2004_03