HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324021Generated: October 28, 2026
Ethylene Glycol → HCID 22007442, compound
https://huagongshe.com/reaction/324021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 10105136 | HCID 10105136 | — |
| Reactant | HCID 10499321 | HCID 10499321 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22007442 | HCID 22007442 | — |
Reaction Steps
A mixture of 1-(2-hydrazino-4-pyridyl)-2,3-bis(hydroxymethyl)-6-methoxy-7-ethoxynaphthalene (2.0 a), (2-carboxyphenyl)-(3-pyridyl) ketone (1.35 g) and ethylene glycol (5 ml) is refluxed for two hours. The mixture under refluxing is cooled to room temperature, and then thereto are added methylene chloride and water. The methylene chloride layer is separated, washed, dried, concentrated under reduced pressure to remove the solvent, and crystallized from chloroform. The precipitated crystals are dissolved in a mixture of chloroform and methanol, and thereto is added a 4 M solution of hydrogen chloride in dioxane (0.67 ml) to give 1-[2-{4-(3-pyridyl)-1(2H)-phthalazinon-2-yl}-4-pyridyl]-2,3-bis(hydroxymethyl)-6-methoxy-7-ethoxynaphthalene hydrochloride (1.43 g), which is listed in Table 10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06214996B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-13a462292d214ad48020f5a7c188bfc1 |
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| Source note | uspto-grants-2001_04 |
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