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N-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamide → 6-ethyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide

HRID 645366
ノート
印刷プレビュー

反応式

HRID 645366 の反応式
[C:1]1([NH:7][C:8]([C:10]2[N:11]=[C:12]3[CH:17]=[CH:16][C:15]([CH:18]=[CH2:19])=[CH:14][N:13]3[CH:20]=2)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H][H]>CO.[Pd]>[CH2:18]([C:15]1[CH:16]=[CH:17][C:12]2[N:13]([CH:20]=[C:10]([C:8]([NH:7][C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)=[O:9])[N:11]=2)[CH:14]=1)[CH3:19]
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 2

HCID 24771613N-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamideHCID 178418361HCID 178418361、化合物

生成物 1

HCID 247716146-ethyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide収率 99.2%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A solution of 60 mg of N-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamide in 15 ml of methanol is hydrogenated at 25° C. for 45 minutes under 1 bar of hydrogen in the presence of 24 mg of 10% palladium-on-charcoal. As the reaction is incomplete, the product is recycled under the same conditions. After filtering, the reaction mixture is concentrated to dryness under reduced pressure. The residue is taken up in 50 ml of ethyl acetate. The organic phase is washed with water, separated by settling, dried and concentrated to dryness under reduced pressure to give 60 mg of 6-ethyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid.

後処理

  1. filtrationAfter filtering
  2. concentrationthe reaction mixture is concentrated to dryness under reduced pressure
  3. washThe organic phase is washed with water
  4. customseparated
  5. customdried
  6. concentrationconcentrated to dryness under reduced pressure

出典と根拠

ORDレコード
ord-59f0bdf5cc2e4e1bbbf01be03e22a18e
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07704989B2

反応ノート

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