Phosphorus oxychloride → 1-Chloro-3-(2,5-dimethoxyphenyl)isoquinoline

HRID 1251102노트

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HRID 1251102 반응식
[CH3:1][NH:2][C:3]([C:5]1[C:6]([CH3:11])=[CH:7][CH:8]=[CH:9][CH:10]=1)=O.[CH3:12][O:13][C:14]1[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[CH:18][C:15]=1C#N.P(Cl)(Cl)([Cl:26])=O>>[Cl:26][C:3]1[C:5]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:11]=[C:1]([C:20]2[CH:21]=[C:14]([O:13][CH3:12])[CH:15]=[CH:18][C:19]=2[O:22][CH3:23])[N:2]=1

참가 물질

4

실험 절차

3-(2,5-Dimethoxyphenyl)isoquinolin-1-one (0.61 g) obtained by reacting N-methyl-o-toluamide (1.64 g) and 2,5-dimethoxybenzonitrile (1.80 g) according to Example 10-1 was reacted with phosphorous oxychloride (10 ml) according to Example 10-2, to give 1-chloro-3-(2,5-dimethoxyphenyl)isoquinoline, which was then reacted with N-ethylpiperazine (15 ml) at 100° C. for 8 hr. The reaction solution was evaporated, and to the resulting residue were added ethyl acetate and water. The resulting organic layer was washed with water and brine, and then dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (methylene chloride/methanol system), to give the free compound of the title compound as a pale yellow oil.

출처 및 근거

ORD 기록
ord-da7efd7f792f437392d54fb81ba6a728
출처 데이터셋
uspto-grants-2002_01
특허 번호
US06340759B1

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