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Pyridine → HCID 15168935, 화합물

HRID 1078554
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인쇄 미리보기

반응식

HRID 1078554 반응식
Cl[C:2]1[C:7]([C:8]([NH:10][C:11]2[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][C:12]=2[OH:18])=[O:9])=[CH:6][C:5]([N+:19]([O-:21])=[O:20])=[CH:4][N:3]=1.N1C=CC=CC=1>O>[N+:19]([C:5]1[CH:4]=[N:3][C:2]2[O:18][C:12]3[CH:13]=[C:14]([CH3:17])[CH:15]=[CH:16][C:11]=3[NH:10][C:8](=[O:9])[C:7]=2[CH:6]=1)([O-:21])=[O:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1049PyridineHCID 15168934HCID 15168934, 화합물

생성물 1

HCID 15168935HCID 15168935, 화합물수율 79.3%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
90 °C

실험 절차

A mixture of 2-chloro-5-nitro-N-(3-hydroxytol-4-yl)-3-pyridinecarboxamide (6.3 g, 0.02 mol) and pyridine (100 ml) was heated under argon at 90° C. for 2.5 hours. The cooled solution was diluted with water and the yellow-orange precipitate collected and washed with water. The solid was then stirred in hot water (100 ml) for 45 min., filtered and washed with ethanol and ether to give 4.3 g of a tan-brown solid. Recrystallization from dimethylformamide/water afforded 3.76 g (69% of theory) of product.

후처리

  1. customthe yellow-orange precipitate collected
  2. washwashed with water
  3. filtrationfiltered
  4. washwashed with ethanol and ether

출처 및 근거

ORD 기록
ord-b60f204d8643434ca12004f710475706
출처 데이터셋
uspto-grants-1996_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05550122

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