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Ammonia → HCID 20142073, 화합물

HRID 649116
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HRID 649116 반응식
[NH3:1].[Cl:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[C:8]([O:13][C:14]3[CH:27]=[CH:26][C:17]([O:18][CH:19]([CH3:25])[C:20](OCC)=[O:21])=[CH:16][CH:15]=3)[CH:9]=[N:10]2)=[CH:5][CH:4]=1>CC(C)=O>[Cl:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[C:8]([O:13][C:14]3[CH:27]=[CH:26][C:17]([O:18][CH:19]([CH3:25])[C:20]([NH2:1])=[O:21])=[CH:16][CH:15]=3)[CH:9]=[N:10]2)=[CH:5][CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 13079890HCID 13079890, 화합물

생성물 1

HCID 20142073HCID 20142073, 화합물

시약·촉매·용매 1

HCID 180Acetone용매

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온도
60 °C

실험 절차

Concentrated ammonia was added at 20° C. to a solution of ethyl 2-[4-(7-chloroquinolin-3-yloxy)phenoxy]propionate (3.0 g) (see Example 5) in acetone (50 ml) until the mixture just began to turn cloudy. The mixture was then heated at 60° C. for 8 hours and allowed to cool and stand overnight. Colourless crystals (1.5 g) 2-[4-(7-chloroquinolin-3-yloxy)phenoxy]propionamide were collected by filtration. The compound was characterised by its proton magnetic resonance spectrum. (Table 3).

후처리

  1. temperatureto cool
  2. filtrationColourless crystals (1.5 g) 2-[4-(7-chloroquinolin-3-yloxy)phenoxy]propionamide were collected by filtration

출처 및 근거

ORD 기록
ord-f387d6d948d24d32a9e46b2ee9ea0e2f
출처 데이터셋
uspto-grants-1988_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04738710

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