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Ethanolamine → 6-Dimethylamino-4-(beta-hydroxyethylamino)quinoline

HRID 550884
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반응식

HRID 550884 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([N:12]([CH3:14])[CH3:13])[CH:10]=2)[N:5]=[CH:4][CH:3]=1.[NH2:15][CH2:16][CH2:17][OH:18].[OH-].[Na+]>O>[CH3:13][N:12]([CH3:14])[C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][CH:8]=1)[N:5]=[CH:4][CH:3]=[C:2]2[NH:15][CH2:16][CH2:17][OH:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 700EthanolamineHCID 14798Sodium HydroxideHCID 436172264-chloro-N,N-dimethylquinolin-6-amine

생성물 1

HCID 671895216-Dimethylamino-4-(beta-hydroxyethylamino)quinoline수율 88%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 4-chloro-6-dimethylaminoquinoline 12 (4.92 g, 24 mmol), prepared according to the method described by Riegel et al., J. Am. Chem. Soc., 1946, 68, 1264, and of 2-aminoethanol (43.99 g, 720 mmol) is heated, with magnetic stirring, at 150° C. for 15 min and then at 185° C. for 30 min. After returning to ambient temperature, the solid is suspended in 25 ml of a 10%, w/v, aqueous sodium hydroxide solution and 165 ml of water. The precipitate obtained is filtered through sintered glass, washed with water and then dried under vacuum. The product is obtained in the form of a white powder: 4.86 g (yield=88%).

후처리

  1. customprepared
  2. customAfter returning to ambient temperature
  3. customThe precipitate obtained
  4. filtrationis filtered through sintered glass
  5. washwashed with water
  6. customdried under vacuum
  7. customThe product is obtained in the form of a white powder

출처 및 근거

ORD 기록
ord-1e26f6f577354dbba12349ce537f700b
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07947701B2

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