Hydrochloric Acid → 2-Amino-3,5-difluoro-6-(methylamino)pyridine

HRID 368409ノート

反応式

HRID 368409 の反応式
Cl.[CH2:2]([NH:9][C:10]1[C:15]([F:16])=[CH:14][C:13]([F:17])=[C:12]([NH:18]C)[N:11]=1)C1C=CC=CC=1>[Pd].CO>[NH2:18][C:12]1[C:13]([F:17])=[CH:14][C:15]([F:16])=[C:10]([NH:9][CH3:2])[N:11]=1

参加物

5

実験手順

To a mixed solution of 10 ml of methanol and 1 ml of concentrated hydrochloric acid were added all amount of the above described 2-benzylamino-3,5-difluoro-6-(methylamino)pyridine together with 0.55 g of 10% palladium on carbon, and the mixture was hydrogenated at 50° C. overnight. The catalyst was separated by filtration, and the solvent and the like were distilled off under reduced pressure. To the residue was added 50 ml of chloroform, and the mixture was washed with 50 ml of 5% aqueous solution of sodium carbonate. The chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The solid precipitate was collected by filtration to obtain 840 mg of the title compound as a pale gray solid.

後処理

  1. customThe catalyst was separated by filtration
  2. distillationthe solvent and the like were distilled off under reduced pressure
  3. additionTo the residue was added 50 ml of chloroform
  4. washthe mixture was washed with 50 ml of 5% aqueous solution of sodium carbonate
  5. dry with materialThe chloroform layer was dried over anhydrous magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. filtrationThe solid precipitate was collected by filtration

出典と根拠

ORDレコード
ord-b3b330d0226442de8f1f3f0bd5dc0b4c
出典データセット
uspto-grants-2000_10
特許番号
US06133284

反応ノート

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