Hydrochloric Acid → [5-(Methanesulfonyl)pyridin-2-yl]methanaminium chloride

HRID 1517475ノート

反応式

HRID 1517475 の反応式
[CH3:1][S:2]([C:5]1[CH:6]=[CH:7][C:8]([C:11]#[N:12])=[N:9][CH:10]=1)(=[O:4])=[O:3].C(O)C.[ClH:16]>[Pd].O>[ClH:16].[CH3:1][S:2]([C:5]1[CH:6]=[CH:7][C:8]([CH2:11][NH2:12])=[N:9][CH:10]=1)(=[O:4])=[O:3]

参加物

6

実験手順

To 5-Methanesulfonyl-pyridine-2-carbonitrile (22 kg, 1.0 mol eq, limiting reagent) was charged palladium on carbon (2.0 kg, 5% w/w), ethanol (110 L, 5 rel vol), water (14 L, 0.64 rel vol) and hydrochloric acid (25.04 kg, 32% w/w). An ethanol line rinse (16 L, 0.7 rel vol) followed. The reaction mixture was heated and subjected to an atmosphere of hydrogen until the reaction was complete as judged by HPLC analysis. Water (108 L, 4.9 rel vol) was charged, the catalyst filtered off and washed with water (36 L, 1.6 rel vol). The combined filtrates were concentrated under reduced pressure to approximately 2.5 rel vols. The reaction was then heated and ethanol (126.3 L, 5.7 rel vol) was charged. The reaction mixture was cooled, stirred and isolated by filtration. The solid was washed with ethanol (73.7 L, 3.3 rel vol) and dried to constant weight to yield the title compound (20.1 kg, 9.05 mol, 82%).

後処理

  1. washAn ethanol line rinse (16 L, 0.7 rel vol)
  2. temperatureThe reaction mixture was heated
  3. additionWater (108 L, 4.9 rel vol) was charged
  4. filtrationthe catalyst filtered off
  5. washwashed with water (36 L, 1.6 rel vol)
  6. concentrationThe combined filtrates were concentrated under reduced pressure to approximately 2.5 rel vols
  7. temperatureThe reaction was then heated
  8. additionethanol (126.3 L, 5.7 rel vol) was charged
  9. temperatureThe reaction mixture was cooled
  10. customisolated by filtration
  11. washThe solid was washed with ethanol (73.7 L, 3.3 rel vol)
  12. customdried to constant weight

出典と根拠

ORDレコード
ord-2c59dadcfc81430ead672d280b550fa9
出典データセット
uspto-grants-2012_07
特許番号
US08232296B2

反応ノート

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