HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-[6,7-Dimethoxyphthalazin-1-yl]piperid-4-one trimethylene ketal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Chloro-6,7-dimethoxyphthalazine | HCID 20511177 | — |
| Reactant | 1,5-Dioxa-9-aza-spiro[5.5]undecane, hydrochloride | HCID 45158781 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[6,7-Dimethoxyphthalazin-1-yl]piperid-4-one trimethylene ketal | HCID 57316590 | 71.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04289772 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-c282c212466d43ef95003ab8a714155e |
| Source note | uspto-grants-1981_09 |