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Morpholine → 5-Morpholin-4-yl-8-nitro-quinoline

HRID 513812
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인쇄 미리보기

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HRID 513812 반응식
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.Cl[C:8]1[CH:17]=[CH:16][C:15]([N+:18]([O-:20])=[O:19])=[C:14]2[C:9]=1[CH:10]=[CH:11][CH:12]=[N:13]2>CS(C)=O.O>[N:1]1([C:8]2[CH:17]=[CH:16][C:15]([N+:18]([O-:20])=[O:19])=[C:14]3[C:9]=2[CH:10]=[CH:11][CH:12]=[N:13]3)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1
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참가 물질

5

반응물 2

HCID 8083MorpholineHCID 2427555-Chloro-8-nitroquinoline

생성물 1

HCID 31356775-Morpholin-4-yl-8-nitro-quinoline수율 81%

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매HCID 962Water용매

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온도
100 °C

실험 절차

Morpholine (251.6 μl, 2.88 mmol) was added to a solution of 5-chloro-8-nitro-quinoline 27 (200 mg, 0.96 mmol) in DMSO (2 ml) and the mixture was heated at 100° C. in a sealed tube for 18 h. After cooling, the mixture was diluted with water (10 ml) and the resulting precipitate was collected by filtration. The solid was dried in vacuo to give the title compound (200 mg, 81%) which was used in the next step without further purification.

후처리

  1. temperatureAfter cooling
  2. filtrationthe resulting precipitate was collected by filtration
  3. customThe solid was dried in vacuo

출처 및 근거

ORD 기록
ord-8b21dc6578694e09b9d724d9dd8b2d68
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102688B2

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