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Ethoxyacetyl chloride → HCID 57429982, 화합물

HRID 2105477
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HRID 2105477 반응식
[CH2:1]([O:3][CH2:4][C:5](Cl)=[O:6])[CH3:2].[NH2:8][C:9]1[CH:10]=[N:11][C:12]2[C:17]([C:18]=1[Cl:19])=[CH:16][CH:15]=[CH:14][CH:13]=2>ClCCl>[Cl:19][C:18]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]=[CH:10][C:9]=1[NH:8][C:5](=[O:6])[CH2:4][O:3][CH2:1][CH3:2]
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참가 물질

4

반응물 2

HCID 84189Ethoxyacetyl chloride2회HCID 8173324-Chloroquinolin-3-amine

생성물 1

HCID 57429982HCID 57429982, 화합물수율 95.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

A solution of ethoxyacetyl chloride (4.2 g, 34 mmol) in dichloromethane was added dropwise to a stirred solution of 3-amino-4-chloroquinoline (5.1 g, 29 mmol) in dichloromethane (75 mL), and the reaction was stirred for one hour at room temperature. Additional ethoxyacetyl chloride (0.5 g, 4 mmol) was added, and the reaction was stirred for 30 minutes and diluted with dichloromethane (75 mL). The resulting mixture was washed with saturated aqueous sodium bicarbonate (50 mL), dried over potassium carbonate, and filtered. Methanol was added to facilitate the filtration. The filtrate was concentrated under reduced pressure to provide 7.3 g of N-(4-chloroquinolin-3-yl)-2-ethoxyacetamide as a dark solid.

후처리

  1. stirringthe reaction was stirred for 30 minutes
  2. washThe resulting mixture was washed with saturated aqueous sodium bicarbonate (50 mL)
  3. dry with materialdried over potassium carbonate
  4. filtrationfiltered
  5. additionMethanol was added
  6. filtrationthe filtration
  7. concentrationThe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-7e3f414f7cef43829d260a441d4acb6e
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07579359B2

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