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Ammonium Hydroxide → 1-(2-Aminopyridin-5-yl)ethanone

HRID 633738
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인쇄 미리보기

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HRID 633738 반응식
Cl[C:2]1[N:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][CH:3]=1.[OH-].[NH4+:12]>>[NH2:12][C:2]1[N:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 14923Ammonium HydroxideHCID 27796981-(6-Chloropyridin-3-yl)ethan-1-one

생성물 1

HCID 211133961-(2-Aminopyridin-5-yl)ethanone

반응 조건

온도
130 °C

실험 절차

2 g (11.57 mmol) of 1-(6-chloropyrid-3-yl)ethanone and 70 mL of ammonium hydroxide are placed in a Parr reactor. The solution is heated at 130° C. overnight. The mixture obtained is evaporated to dryness, and the residue is taken up in ethyl acetate and washed with water and with saturated NaCl solution. The organic phase is dried over sodium sulfate and evaporated to dryness to give 1.14 g of 1-(6-aminopyrid-3-yl)ethanone, the characteristics of which are as follows:

후처리

  1. customThe mixture obtained
  2. customis evaporated to dryness
  3. washwashed with water and with saturated NaCl solution
  4. dry with materialThe organic phase is dried over sodium sulfate
  5. customevaporated to dryness

출처 및 근거

ORD 기록
ord-bb41f7a833024d76b26c12616ecec026
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09321790B2

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