HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814457Generated: November 3, 2026
Hydroxyamine hydrochloride → HCID 135719043, compound
https://huagongshe.com/reaction/1814457
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 22502996 | HCID 22502996 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 135719043 | HCID 135719043 | — |
| Product | HCID 136119044 | HCID 136119044 | — |
Reaction Steps
1-(4-Ethylpiperazin-1-yl)-3-(4-formylphenyl)isoquinoline (3.00 g) obtained in Example 17-5 was reacted with hydroxylamine hydrochloride (0.90 g) and sodium acetate (1.10 g) in ethanol (50 ml) at 60° C. for 2 hr. The reaction solution was evaporated, and then the resulting residue was extracted in methylene chloride, washed with brine and dried. The solvent was removed, and the resulting residue was isolated and purified by silica gel column chromatography (methylene chloride/methanol system), to give (Z)-1-(4-ethylpiperazin-1-yl)-3-(4-hydroxyiminomethylphenyl)isoquinoline (1.01 g) and (E)-1-(4-ethylpiperazin-1-yl)-3-(4-hydroxyiminomethylphenyl)isoquinoline (1.52 g), both as yellow solids. 0.30 g each of the compounds was converted into a hydrochloride in a conventional manner, to give the hydrochlorides of the title compounds as yellow powders (0.32 g and 0.35 g, respectively).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875761B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-e534f20d25124886810e400192f289d4 |
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| Source note | uspto-grants-2005_04 |
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