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Anisole → 6-(4-(1H-pyrazol-1-yl)benzyl)-5-methylisoindolin-1-one

HRID 629345
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인쇄 미리보기

반응식

HRID 629345 반응식
[N:1]1([C:6]2[CH:34]=[CH:33][C:9]([CH2:10][C:11]3[CH:19]=[C:18]4[C:14]([CH2:15][N:16](CC5C=CC(OC)=CC=5OC)[C:17]4=[O:20])=[CH:13][C:12]=3[CH3:32])=[CH:8][CH:7]=2)[CH:5]=[CH:4][CH:3]=[N:2]1.C1(OC)C=CC=CC=1>FC(F)(F)C(O)=O>[N:1]1([C:6]2[CH:34]=[CH:33][C:9]([CH2:10][C:11]3[CH:19]=[C:18]4[C:14]([CH2:15][NH:16][C:17]4=[O:20])=[CH:13][C:12]=3[CH3:32])=[CH:8][CH:7]=2)[CH:5]=[CH:4][CH:3]=[N:2]1
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참가 물질

4

반응물 2

HCID 7519AnisoleHCID 1184682936-(4-(1H-pyrazol-1-yl)benzyl)-2-(2,4-dimethoxybenzyl)-5-methylisoindolin-1-one

생성물 1

HCID 1184684536-(4-(1H-pyrazol-1-yl)benzyl)-5-methylisoindolin-1-one수율 93.4%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

반응 조건

온도
80 °C

실험 절차

To a solution of 6-(4-(1H-pyrazol-1-yl)benzyl)-2-(2,4-dimethoxybenzyl)-5-methylisoindolin-1-one (0.24 g) in trifluoroacetic acid (4.34 mL) was added anisole (0.23 mL), and the mixture was stirred at 80° C. for 2 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (0.15 g).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customthe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-2c61fd425dfc464dacdbd648a108aad5
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09315458B2

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