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Potassium Iodide → HCID 86628512、化合物

HRID 546743
ノート
印刷プレビュー

反応式

HRID 546743 の反応式
C(=O)([O-])[O-].[Cs+].[Cs+].[I-].[K+].Cl[CH2:10][C:11](=[O:13])[CH3:12].[Cl:14][C:15]1[N:20]=[C:19]([O:21][CH3:22])[C:18]([NH:23][CH:24]=[O:25])=[CH:17][CH:16]=1>CN(C=O)C.C(Cl)(Cl)Cl>[Cl:14][C:15]1[N:20]=[C:19]([O:21][CH3:22])[C:18]([N:23]([CH2:10][C:11](=[O:13])[CH3:12])[CH:24]=[O:25])=[CH:17][CH:16]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 4875Potassium IodideHCID 6571ChloroacetoneHCID 10796Cesium carbonateHCID 86628511N-(6-chloro-2-methoxypyridin-3-yl)formamide

生成物 1

HCID 86628512HCID 86628512、化合物

試薬・触媒・溶媒 2

HCID 6212Chloroform溶媒
HCID 6228
Dimethylformamide
溶媒

反応条件

温度
100 °C

実験手順

Cesium carbonate (20.5 g), potassium iodide (521 mg) and chloroacetone (5.0 mL) were added to a solution of N-(6-chloro-2-methoxypyridin-3-yl)formamide (5.85 g) in DMF (34.3 mL), and the reaction solution was stirred at 100° C. for one hour. Ice water and chloroform were added to the reaction solution, and the organic layer was separated. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system) to obtain 4.71 g of the title compound. The property value of the compound is as follows.

後処理

  1. customthe organic layer was separated
  2. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system)

出典と根拠

ORDレコード
ord-f16c66df71ce4c2ba39576aca2740a8e
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07935815B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート