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碳酸氢铯 → HCID 86630117,化合物

HRID 1715313
笔记
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反应方程式

HRID 1715313 反应方程式
C(=O)([O-])[O-].[Cs+].[Cs+].CN1CCCC1=O.[Cl:14][C:15]1[C:20]([OH:21])=[CH:19][CH:18]=[CH:17][N:16]=1.Cl[C:23]1[CH:24]=[CH:25][C:26]([S:29]([CH2:32][CH3:33])(=[O:31])=[O:30])=[N:27][CH:28]=1>C(OCC)(=O)C.[Cl-].[NH4+]>[Cl:14][C:15]1[C:20]([O:21][C:23]2[CH:28]=[N:27][C:26]([S:29]([CH2:32][CH3:33])(=[O:30])=[O:31])=[CH:25][CH:24]=2)=[CH:19][CH:18]=[CH:17][N:16]=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

7

反应物 4

HCID 10796碳酸氢铯HCID 13387甲基吡咯烷酮HCID 811362-氯-3-羟基吡啶HCID 231451535-氯-2-(乙硫酰基)吡啶

产物 1

HCID 86630117HCID 86630117,化合物

试剂、催化剂与溶剂 2

HCID 8857乙酸乙酯溶剂HCID 25517氯化铵
溶剂

反应条件

温度
100 °C

实验过程

Cesium carbonate (20 g) was added to an N-methyl-2-pyrrolidinone (160 ml) solution of 2-chloro-3-hydroxypyridine (6 g) and 5-chloro-2-(ethylsulfonyl)pyridine (4.8 g), and stirred at 100° C. for 24 hours. After this was diluted with ethyl acetate, aqueous saturated ammonium chloride solution was added with cooling with ice. The organic layer was washed with water and saturated saline water. After dried, the solvent was evaporated away under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate) to obtain the entitled compound as a brown oil.

后处理

  1. additionwas added
  2. temperaturewith cooling with ice
  3. washThe organic layer was washed with water and saturated saline water
  4. customAfter dried
  5. customthe solvent was evaporated away under reduced pressure
  6. customthe residue was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate)

来源与证据

ORD记录
ord-ec09882111ee49139e4d4cf6afd797be
来源数据集
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
专利号
US07799820B2

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