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Potassium Iodide → HCID 86628512, 화합물

HRID 546743
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HRID 546743 반응식
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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

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

생성물 1

HCID 86628512HCID 86628512, 화합물

시약·촉매·용매 2

HCID 6212Chloroform용매
HCID 6228
Dimethylformamide
용매

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온도
100 °C

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-f16c66df71ce4c2ba39576aca2740a8e
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07935815B2

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