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氢氧化钠 → 4-氯-2-(4-氟苯基氨基)-5,6-二甲基嘧啶

HRID 1069394
笔记
打印预览

反应方程式

HRID 1069394 反应方程式
O[C:2]1[C:7]([CH3:8])=[C:6]([CH3:9])[N:5]=[C:4]([NH:10][C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[N:3]=1.P(Cl)(Cl)([Cl:20])=O.[OH-].[Na+]>CN(C)C=O>[Cl:20][C:2]1[C:7]([CH3:8])=[C:6]([CH3:9])[N:5]=[C:4]([NH:10][C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[N:3]=1
参与物反应条件实验过程后处理来源与证据反应笔记

参与物

5

反应物 3

HCID 14798氢氧化钠HCID 24813三氯氧磷HCID 178433118HCID 178433118,化合物

产物 1

HCID 99923764-氯-2-(4-氟苯基氨基)-5,6-二甲基嘧啶收率 96.7%

试剂、催化剂与溶剂 1

HCID 6228N,N-二甲基甲酰胺溶剂

反应条件

温度
80 °C

实验过程

40.5 g (174.1 mmole) of 2-(4-fluorophenylamino)-4-hydroxy-5,6-dimethylpyrimidine produced in Example 1 was suspended in 80 ml of N,N-dimethylformamide and the resulting suspension was heated to 80° C. 31.9 g (19.4 ml, 210.1 mmole) of phosphorus oxychloride was added thereto over one hour at constant temperature of 85° C. The reaction solution was stirred for 30 minutes and then 400 g of ice-water was added thereto with stirring. The mixture was adjusted to pH 11 by adding sodium hydroxide and then the resulting solid product was filtered. The separated solid product was washed with 150 ml of 50% aqueous methanol solution and then dried to obtain 42.3 g of the title compound.

后处理

  1. stirringwith stirring
  2. filtrationthe resulting solid product was filtered
  3. washThe separated solid product was washed with 150 ml of 50% aqueous methanol solution
  4. customdried

来源与证据

ORD记录
ord-c62cba1c5c884d44a819a00b7e24e16a
来源数据集
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
专利号
US06252076B1

反应笔记

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本页导航参与物反应条件实验过程后处理来源与证据反应笔记