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Water → (R)-1-{4-[4-(4-Tert-butylphenylamino)phenoxy]-6-methoxyquinolin-7-yloxy}-3-morpholin-4-ylpropan-2-ol

HRID 1727866
ノート
印刷プレビュー

反応式

HRID 1727866 の反応式
[C:1]([C:5]1[CH:31]=[CH:30][C:8]([NH:9][C:10]2[CH:29]=[CH:28][C:13]([O:14][C:15]3[C:24]4[C:19](=[CH:20][C:21]([OH:27])=[C:22]([O:25][CH3:26])[CH:23]=4)[N:18]=[CH:17][CH:16]=3)=[CH:12][CH:11]=2)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[C:32](=O)([O-])[O-].[K+].[K+].[NH:38]1[CH2:43][CH2:42][O:41][CH2:40][CH2:39]1.O.C([O:48][CH2:49][CH3:50])(=O)C>CN(C)C=O>[C:1]([C:5]1[CH:31]=[CH:30][C:8]([NH:9][C:10]2[CH:29]=[CH:28][C:13]([O:14][C:15]3[C:24]4[C:19](=[CH:20][C:21]([O:27][CH2:32][C@H:49]([OH:48])[CH2:50][N:38]5[CH2:43][CH2:42][O:41][CH2:40][CH2:39]5)=[C:22]([O:25][CH3:26])[CH:23]=4)[N:18]=[CH:17][CH:16]=3)=[CH:12][CH:11]=2)=[CH:7][CH:6]=1)([CH3:4])([CH3:2])[CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 962WaterHCID 8083MorpholineHCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 1357802514-[4-(4-Tert-butylphenylamino)phenoxy]-6-methoxyquinolin-7-ol2 回

生成物 1

HCID 57567453(R)-1-{4-[4-(4-Tert-butylphenylamino)phenoxy]-6-methoxyquinolin-7-yloxy}-3-morpholin-4-ylpropan-2-ol
収率 65%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

4-[4-(4-Tert-butylphenylamino)phenoxy]-6-methoxyquinolin-7-ol (compound 21) (230 mg) was dissolved in N,N-dimethylformamide (8 ml) to prepare a solution. Potassium carbonate (300 mg) and p-toluenesulfonic acid (2R)-(−)-glycidyl (0.22 g) were then added to the solution, and the mixture was stirred at room temperature overnight. Morpholine (0.5 ml) was added to the reaction solution, and the mixture was further stirred at 70° C. overnight. Water and ethyl acetate were added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and was dried over sodium sulfate. The solvent was removed by evaporation under the reduced pressure, and the residue was purified by thin-layer chromatography on silica gel using chloroform/acetone for development to give the title compound (200 mg, yield 65%).

後処理

  1. customto prepare a solution
  2. stirringthe mixture was further stirred at 70° C. overnight
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe extract was washed with saturated brine
  5. dry with materialwas dried over sodium sulfate
  6. customThe solvent was removed by evaporation under the reduced pressure
  7. customthe residue was purified by thin-layer chromatography on silica gel

出典と根拠

ORDレコード
ord-41655aaf040144808a3bef4bf993779e
出典データセット
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07495104B2

反応ノート

読み込み中…

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