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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPiperidin-3-ylmethanolHCID 107308—
Reactant1-Chloro-6,7-dimethoxyphthalazineHCID 20511177—
SolventIsoamyl AlcoholHCID 31260—
Product6,7-Dimethoxy-1-(3-hydroxymethylpiperidino)phthalazineHCID 2051122560.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04370328
Source datasetuspto-grants-1983_01
ORD IDord-5512212279db4f2db5e13bf7d5899dda
Source noteuspto-grants-1983_01