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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348518Generated: November 1, 2026

Piperidine → HCID 73446802, compound

https://huagongshe.com/reaction/1348518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant(2-tert-Butyl-6-methyl-4H-pyran-4-ylidene)propanedinitrileHCID 15374739—
ReactantHCID 18458012HCID 18458012—
SolventEthanolHCID 702—
ProductHCID 73446802HCID 7344680248.8%

Reaction Conditions

Temperature75 °C

Reaction Steps

As shown in the following reaction 1, 2.14 g (10 mmol) of 2-(2-tert-butyl-6-methyl-pyran-4-ylidene)-malononitrile and 2.13 g (10 mmol) of 7-dimethylamino-2,3-dihydro-thieno[3,4-b][1,4]dioxine-5-carbaldehyde were added into 100 ml of ethanol, and 0.93 g (11 mmol) of piperidine was added thereto. The reaction solution was heated at 75° C. for 10 hours. After cooling the reaction solution, the precipitated red solid was filtered, and recrystallized with ethanol to obtain 2 g of the target compound (Yield 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211335B2
Source datasetuspto-grants-2007_05
ORD IDord-8564b43dc7534184b7697101410e3e8d
Source noteuspto-grants-2007_05