Benzene → N-(1-methoxy-2,2,2-trifluoroethyl)-4-methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamide

HRID 1250500노트

반응식

HRID 1250500 반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([F:19])([F:18])[F:17])[CH:11]=2)[N:6]=[C:5]([C:20]([NH2:22])=[O:21])[CH:4]=1.O.[F:24][C:25]([F:29])([F:28])[CH:26]=[O:27].[CH:30]1C=CC=CC=1>>[CH3:30][O:27][CH:26]([NH:22][C:20]([C:5]1[CH:4]=[C:3]([O:2][CH3:1])[CH:8]=[C:7]([O:9][C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([F:18])([F:19])[F:17])[CH:11]=2)[N:6]=1)=[O:21])[C:25]([F:29])([F:28])[F:24]

참가 물질

4

반응물 3

HCID 241BenzeneHCID 27813662,2,2-Trifluoroacetaldehyde hydrateHCID 183262294-Methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamide

생성물 1

HCID 18326218N-(1-methoxy-2,2,2-trifluoroethyl)-4-methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamide

실험 절차

4-methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamide was dissolved in benzene and mixed with 0.36 g (0.0026×1.2 mol) of trifluoroacetaldehyde hydrate, followed by treating the obtained solution under reflux for about 5 hours. The reaction solution was concentrated and then distributed in ethyl acetate-saturated sodium bicarbonate water, followed by washing with saturated brine. The organic phase of the obtained solution was dried with anhydrous sodium sulfate, concentrated and purified by silica gel column chromatography (eluting solution: ethyl acetate/hexane), thereby obtaining an aimed product.

후처리

  1. additionby treating the obtained solution
  2. temperatureunder reflux for about 5 hours
  3. concentrationThe reaction solution was concentrated
  4. washby washing with saturated brine
  5. dry with materialThe organic phase of the obtained solution was dried with anhydrous sodium sulfate
  6. concentrationconcentrated
  7. custompurified by silica gel column chromatography (eluting solution: ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-e645bd9b7e22498b9d4dcd93fda32a2c
출처 데이터셋
uspto-grants-2002_01
특허 번호
US06339045B1

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