5-iodo-6-phenoxy-2-phenyl-4(3H)-pyrimidinone → 6-phenoxy-2-phenyl-4(3H)-pyrimidinone

HRID 1450

反应方程式

HRID 1450 反应方程式
I[C:2]1[C:3](=[O:21])[NH:4][C:5]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[N:6][C:7]=1[O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>[Zn].C(O)(=O)C>[O:8]([C:7]1[N:6]=[C:5]([C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[NH:4][C:3](=[O:21])[CH:2]=1)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1

参与物

4

反应物 1

HCID 131858385-iodo-6-phenoxy-2-phenyl-4(3H)-pyrimidinone

产物 1

HCID 131858416-phenoxy-2-phenyl-4(3H)-pyrimidinone收率 125.6%

试剂、催化剂与溶剂 2

HCID 23994Zinc催化剂3 次HCID 176醋酸溶剂

实验过程

A mixture of 7.07 g (18.1 mmol) of crude 5-iodo-6-phenoxy-2-phenyl-4(3H)-pyrimidinone, 2.02 g (31.1 mmol) of zinc dust and 25 mL of glacial acetic acid was heated to reflux. After 15 min an additional 2.06 g (31.7 mmol) of zinc dust was added, followed 15 min later by a further 2.04 g (31.4 mmol) of zinc dust. The mixture was maintained at reflux for 2 h, cooled and filtered to remove unreacted zinc. The filtrate was rotovaped to leave a semi-solid which was triturated with 75 mL of boiling water to afford 6.01 g (57% from 4,6-dihydroxy-2-phenylpyrimidine) of 6-phenoxy-2-phenyl-4(3H)-pyrimidinone as a yellow solid. 1H-NMR (d6-DMSO) δ 5.5(1H,s), 7.1-7.5(8H), 8.1(2H).

后处理

  1. temperaturewas heated to reflux
  2. temperatureThe mixture was maintained
  3. temperatureat reflux for 2 h
  4. temperaturecooled
  5. filtrationfiltered
  6. customto remove unreacted zinc
  7. customto leave a semi-solid which
  8. customwas triturated with 75 mL of boiling water

来源与证据

ORD记录
ord-d6194f9ae43e4fbd94964245b6b3d3e4
来源数据集
uspto-grants-1998_03
专利号
US05726124

关联笔记

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