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碘化钾 → 1-(2-嘧啶基)-1,4-二氮杂环庚烷

HRID 1636282
笔记
打印预览

反应方程式

HRID 1636282 反应方程式
[NH:1]1[CH2:7][CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.Cl[C:9]1[N:14]=[CH:13][CH:12]=[CH:11][N:10]=1.C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>C(#N)C>[N:10]1[CH:11]=[CH:12][CH:13]=[N:14][C:9]=1[N:1]1[CH2:7][CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1
参与物实验过程后处理来源与证据反应笔记

参与物

6

反应物 4

HCID 4875碘化钾HCID 11430碳酸钾HCID 68163高哌嗪HCID 744042-氯嘧啶

产物 1

HCID 27724091-(2-嘧啶基)-1,4-二氮杂环庚烷收率 48%

试剂、催化剂与溶剂 1

HCID 6342乙腈溶剂

实验过程

50 ml of acetonitrile was added to 10.0 g (0.1 mole) of homopiperazine, 2.9 g (0.025 mole) of 2-chloropyrimidine, 6.9 g (0.05 mole) of potassium carbonate and a catalytic amount of potassium iodide, and the mixture was refluxed under heating for 11 hours. The mixture was cooled to room temperature and then filtered, the filtrate obtained was concentrated under reduced pressure, and the residue was applied to silica gel column chromatography (eluent; a chloroform:methanol=8:2 mixed solution) to obtain 2.14 g of 1-(2-pyrimidyl)homopiperazine as a pale yellow liquid.

后处理

  1. temperatureunder heating for 11 hours
  2. filtrationfiltered
  3. customthe filtrate obtained
  4. concentrationwas concentrated under reduced pressure

来源与证据

ORD记录
ord-dd1f95b2fd884e55b18f349aa1d75c39
来源数据集
uspto-grants-2000_03
DOI
10.6084/m9.figshare.5104873.v1
专利号
US06034086

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记