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Ammonia → 2,5-Dichloro-3,6-difluoropyridin-4-amine

HRID 368458
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HRID 368458 반응식
C(Cl)(Cl)Cl.[Cl:5][C:6]1[C:11]([F:12])=[C:10]([N:13]2C(=O)C3=CC=CC=C3C2=O)[C:9]([Cl:24])=[C:8]([F:25])[N:7]=1.N>CO>[NH2:13][C:10]1[C:9]([Cl:24])=[C:8]([F:25])[N:7]=[C:6]([Cl:5])[C:11]=1[F:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 222AmmoniaHCID 6212ChloroformHCID 22121238N-(2,5-dichloro-3,6-difluoropyridin-4-yl)phthalimide

생성물 1

HCID 221211852,5-Dichloro-3,6-difluoropyridin-4-amine수율 46.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a mixed solution of 100 ml chloroform and 40 ml methanol was added 16.2 g of N-(2,5-dichloro-3,6-difluoropyridine-4-yl)phthalimide together with 20 ml of 25% aqueous solution of ammonia, and the mixture was stirred at room temperature for 30 minutes. The solution was concentrated under reduced pressure, and after adding 150 ml of chloroform to the residue, the mixture was washed with 20 ml of 15% aqueous solution of ammonia, and then, with 10 ml of distilled water. The chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 4.55 g of the title compound as a colorless powder.

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후처리

  1. concentrationThe solution was concentrated under reduced pressure
  2. additionafter adding 150 ml of chloroform to the residue
  3. washthe mixture was washed with 20 ml of 15% aqueous solution of ammonia
  4. dry with materialThe chloroform layer was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-6c989c29086a4596b78b600fa1689c51
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06133284

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