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

HRID 368458
ノート
印刷プレビュー

反応式

HRID 368458 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-6c989c29086a4596b78b600fa1689c51
出典データセット
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06133284

反応ノート

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