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5-Chloro-2-methoxy-3-nitropyridine → 5-Chloro-2-methoxypyridin-3-amine

HRID 2279078
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HRID 2279078 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([N+:10]([O-])=O)[C:5]([O:8][CH3:9])=[N:6][CH:7]=1>[Pt].C(OCC)(=O)C.[Br-].[Zn+2].[Br-]>[Cl:1][C:2]1[CH:3]=[C:4]([NH2:10])[C:5]([O:8][CH3:9])=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 263702185-Chloro-2-methoxy-3-nitropyridine

생성물 1

HCID 451221815-Chloro-2-methoxypyridin-3-amine수율 102.6%

시약·촉매·용매 3

HCID 23939Platinum촉매HCID 10421208Zinc bromide촉매HCID 8857Ethyl Acetate용매

실험 절차

Zinc bromide (226 mg, 1 mmol) and platinum on carbon (5%, 491 mg, 2.52 mmol) were added to a solution of 5-chloro-2-methoxy-3-nitropyridine (Preparation 23a, 950 mg, 5.04 mmol) in ethyl acetate (15 mL) and the reaction mixture was stirred at ambient temperature for 5 hours under a hydrogen atmosphere. The mixture was then filtered through Celite® and the filter cake was washed with methanol. The combined filtrate and washings were concentrated to give the title compound (820 mg, 100%) as a white solid.

후처리

  1. filtrationThe mixture was then filtered through Celite®
  2. washthe filter cake was washed with methanol
  3. concentrationThe combined filtrate and washings were concentrated

출처 및 근거

ORD 기록
ord-c22281cbf1d44ae4b973e6e0045781fd
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133200B2

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