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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577834Generated: November 3, 2026

Triethylamine → 1-[6,7-Dimethoxyphthalazin-1-yl]piperid-4-one trimethylene ketal

https://huagongshe.com/reaction/1577834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Chloro-6,7-dimethoxyphthalazineHCID 20511177—
Reactant1,5-Dioxa-9-aza-spiro[5.5]undecane, hydrochlorideHCID 45158781—
SolventEthanolHCID 702—
Product1-[6,7-Dimethoxyphthalazin-1-yl]piperid-4-one trimethylene ketalHCID 5731659071.5%

Reaction Steps

4-Piperidone trimethylene ketal hydrochloride (20 g), 1-chloro-6,7-dimethoxyphthalazine (10 g), triethylamine (50 ml) and ethanol (300 ml) were heated together under reflux for 70 hours. The resulting mixture was evaporated in vacuo and the residue was partitioned between chloroform (2×100 ml) and water (60 ml). The chloroform extracts were combined, dried (MgSO4) and evaporated in vacuo to give a crude brown oil which on trituration with ethyl acetate (100 ml) at boiling point gave 1-[6,7-dimethoxyphthalazin-1-yl]piperid-4-one trimethylene ketal (11 g), m.p. 194°-6°. A second crop of the product (3 g) was obtained by evaporating the ethyl acetate trituration liquors.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04289772
Source datasetuspto-grants-1981_09
ORD IDord-c282c212466d43ef95003ab8a714155e
Source noteuspto-grants-1981_09