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Water → 6-(Morpholine-4-carbonyl)-3,4-dihydroquinolin-2(1H)-one

HRID 1153980
ノート
印刷プレビュー

反応式

HRID 1153980 の反応式
[NH:1]1[C:11]2[C:6](=[CH:7][C:8]([C:12]([O-:14])=O)=[CH:9][CH:10]=2)[CH2:5][CH2:4][C:2]1=[O:3].[NH:15]1[CH2:20][CH2:19][O:18][CH2:17][CH2:16]1.O>CN(C)C=O>[O:18]1[CH2:19][CH2:20][N:15]([C:12]([C:8]2[CH:7]=[C:6]3[C:11](=[CH:10][CH:9]=2)[NH:1][C:2](=[O:3])[CH2:4][CH2:5]3)=[O:14])[CH2:16][CH2:17]1
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 3

HCID 962WaterHCID 8083MorpholineHCID 71319083,4-Dihydrocarbostyril-6-carboxylate

生成物 1

HCID 131953376-(Morpholine-4-carbonyl)-3,4-dihydroquinolin-2(1H)-one

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

1.0 Gram of succenimide 3,4-dihydrocarbostyril-6-carboxylate and 0.37 g of morpholine were dissolved in 2 ml of dimethylformamide and stirred at room temperature for 3 hours. Then water was added to the reaction mixture and extracted with chloroform, the chloroform layer was washed with water and a saturated sodium chloride aqueous solution in this order. After drying the chloroform layer with anhydrous sodium sulfate, then chloroform was removed by distillation under a reduced pressure, then acetone was added to the thus obtained residue to crystallize the product. 150 Milligrams of 6-morpholinocarbonyl-3,4-dihydrocarbostyril was obtained. Colorless granular crystals. Melting point: 206°-207° C. (from ethanol).

後処理

  1. extractionextracted with chloroform
  2. washthe chloroform layer was washed with water
  3. dry with materialAfter drying the chloroform layer with anhydrous sodium sulfate
  4. customchloroform was removed by distillation under a reduced pressure
  5. additionacetone was added to the thus obtained residue
  6. customto crystallize the product

出典と根拠

ORDレコード
ord-fa449936dda14a3d96759f870e25be01
出典データセット
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04487772

反応ノート

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