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

HRID 2055006
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반응식

HRID 2055006 반응식
[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
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참가 물질

5

반응물 2

HCID 11430Potassium CarbonateHCID 219488002-(Morpholin-4-ylmethyl)-5-nitroquinoline

생성물 1

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

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-d8af3d6575ac44c2881f5fbe604cc5f9
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07329753B2

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