HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251102Generated: October 25, 2026
Phosphorus oxychloride → 1-Chloro-3-(2,5-dimethoxyphenyl)isoquinoline
https://huagongshe.com/reaction/1251102
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N-methyl-2-toluamide | HCID 75111 | — |
| Reactant | 2,5-Dimethoxybenzonitrile | HCID 79200 | — |
| Product | 1-Chloro-3-(2,5-dimethoxyphenyl)isoquinoline | HCID 22502831 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06340759B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-da7efd7f792f437392d54fb81ba6a728 |
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| Source note | uspto-grants-2002_01 |
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