HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164507Generated: October 27, 2026
Triethylamine → 6,7-Dimethoxy-1-(3-hydroxymethylpiperidino)phthalazine
https://huagongshe.com/reaction/1164507
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Piperidin-3-ylmethanol | HCID 107308 | — |
| Reactant | 1-Chloro-6,7-dimethoxyphthalazine | HCID 20511177 | — |
| Solvent | Isoamyl Alcohol | HCID 31260 | — |
| Product | 6,7-Dimethoxy-1-(3-hydroxymethylpiperidino)phthalazine | HCID 20511225 | 60.2% |
Reaction Steps
1-Chloro-6,7-dimethoxy phthalazine (2.25 g.), 3-hydroxymethylpiperidine (1.72 g.) and triethylamine (1.3 ml.) in iso-amyl alcohol (60 ml.) were heated at 95° C. for 42 hours. The cooled reaction mixture was then filtered and the filtrate was taken to dryness in vacuo. The residue was dissolved in water (100 ml.), 5 N sodium hydroxide solution was added to give a pH of 11 and the basic mixture was then extracted with chloroform (2×100 ml.). The chloroform extracts were combined, dried (MgSO4) and concentrated in vacuo to give a brown oil, which was triturated with ether (50 ml.) and filtered. The resultant solid was crystallized twice from acetonitrile, yielding 6,7-dimethoxy-1-(3-hydroxymethylpiperidino)phthalazine (1.83 g.), m.p. 162°-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04370328 |
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| Source dataset | uspto-grants-1983_01 |
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| ORD ID | ord-5512212279db4f2db5e13bf7d5899dda |
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| Source note | uspto-grants-1983_01 |
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