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Potassium Carbonate → 5-Amino-2-(morpholin-4-ylmethyl)quinoline

HRID 2055006
ノート
印刷プレビュー

反応式

HRID 2055006 の反応式
[N:1]1([CH2:7][C:8]2[CH:17]=[CH:16][C:15]3[C:10](=[CH:11][CH:12]=[CH:13][C:14]=3[N+:18]([O-])=O)[N:9]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.C(=O)([O-])[O-].[K+].[K+]>CO.[Pd]>[NH2:18][C:14]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:15]=1[CH:16]=[CH:17][C:8]([CH2:7][N:1]1[CH2:2][CH2:3][O:4][CH2:5][CH2:6]1)=[N:9]2
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 11430Potassium CarbonateHCID 219488002-(Morpholin-4-ylmethyl)-5-nitroquinoline

生成物 1

HCID 219488345-Amino-2-(morpholin-4-ylmethyl)quinoline

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

190 mg (0.7 mmol) of 2-(morpholin-4-ylmethyl)-5-nitroquinoline is dissolved in 10 ml of methanol. After the addition of 19 mg of palladium on carbon and 19 mg of potassium carbonate, the reaction mixture is allowed to stir for 4 hours at room temperature under hydrogen atmosphere. It is then filtered on Celite and washed with ethyl acetate. After removal of the solvent in a vacuum and chromatography on silica gel with hexane-ethyl acetate (0-100%) as well as with ethyl acetate-methanol (0-100%), 134 mg (79% of theory) of the product is obtained.

後処理

  1. filtrationIt is then filtered on Celite
  2. washwashed with ethyl acetate
  3. customAfter removal of the solvent in a vacuum and chromatography on silica gel with hexane-ethyl acetate (0-100%) as well as with ethyl acetate-methanol (0-100%), 134 mg (79% of theory) of the product
  4. customis obtained

出典と根拠

ORDレコード
ord-d8af3d6575ac44c2881f5fbe604cc5f9
出典データセット
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07329753B2

反応ノート

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