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Water → 5-Bromo-2-ethoxypyridin-3-amine

HRID 1052519
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HRID 1052519 반응식
[Br:1][C:2]1[CH:3]=[C:4]([N+:11]([O-])=O)[C:5]([O:8][CH2:9][CH3:10])=[N:6][CH:7]=1.[Cl-].[NH4+].O>CCO.[Fe]>[Br:1][C:2]1[CH:3]=[C:4]([NH2:11])[C:5]([O:8][CH2:9][CH3:10])=[N:6][CH:7]=1
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참가 물질

6

반응물 3

HCID 962WaterHCID 25517Ammonium ChlorideHCID 582557825-Bromo-2-ethoxy-3-nitropyridine

생성물 1

HCID 532116995-Bromo-2-ethoxypyridin-3-amine수율 83%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 702Ethanol용매

실험 절차

5-Bromo-2-ethoxy-3-nitropyridine (805 mg, 3.26 mmol), ammonium chloride (732 mg, 13.68 mmol) and powdered iron (764 mg, 13.68 mmol) were suspended in EtOH (3.4 ml) and water (3.4 ml) and stirred for 90 min at 100° C. The reaction mixture was filtered through Celite after dilution with EtOH. The solvent was evaporated under reduced pressure, water was added and the mixture neutralised to pH=6 with sodium carbonate and extracted with dichloromethane (×3). The organic phase was washed successively with water and brine, dried over magnesium sulphate, filtered and the solvent evaporated under reduced pressure. 708 mg (83% yield, 92% purity) of the titled compound were obtained and used in the next synthetic step without further purification.

후처리

  1. filtrationThe reaction mixture was filtered through Celite after dilution with EtOH
  2. customThe solvent was evaporated under reduced pressure, water
  3. additionwas added
  4. extractionextracted with dichloromethane (×3)
  5. washThe organic phase was washed successively with water and brine
  6. dry with materialdried over magnesium sulphate
  7. filtrationfiltered
  8. customthe solvent evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-46a3667688f6494dba172097cb605658
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09388189B2

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