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

HRID 1814445노트

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HRID 1814445 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 phosphorus 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-0f36c48cb09744f39670e6f72b3c52f0
출처 데이터셋
uspto-grants-2005_04
특허 번호
US06875761B2

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