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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429049Generated: October 29, 2026

Triethylamine → HCID 20703336, compound

https://huagongshe.com/reaction/429049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPiperidin-4-olHCID 79341—
Reactant6,9-dichloro-3-ethyl-3H-pyrazolo[4',3':5,6]pyrido[3,4-d]pyridazineHCID 10869253—
SolventTetrahydrofuran ethanolHCID 21873804—
ProductHCID 20703336HCID 2070333680%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 6,9-dichloro-3-ethyl-3H-pyrazolo[4′,3′:5,6]pyrido[3,4-d]pyridazine (3.2 g, 12.0 mmol) in THF/ethanol (40 mL, 1:1) in a 100 mL pressure tube was added triethylamine (5 eq) and 4-hydroxy-piperidine (1.1 eq) sequentially. The reaction mixture was heated in an oil bath at 60° C. for 2 h. The progress of the reaction was monitored by HPLC. The reaction mixture was transferred to a 200 mL round-bottomed flask, and the solvent was removed via evaporation under reduced pressure. The light brown residue was resuspended in saturated sodium bicarbonate (100 mL), and the precipitated solid was collected by filtration. This orange solid was washed thoroughly with water and dried in a vacuum oven at 40° C. over night to afford the title compound (3.2 g, 80% yield). This material was >93% pure and was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316438B1
Source datasetuspto-grants-2001_11
ORD IDord-8c9927d37c7b4117aeb9f24bed0d9c04
Source noteuspto-grants-2001_11