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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366379Generated: November 4, 2026

Piperidine → HCID 11965417, compound

https://huagongshe.com/reaction/2366379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3,4-DimethoxybenzeneacetonitrileHCID 66727—
Reactant5-Bromofuran-2-carbaldehydeHCID 600328—
Reactant5-Piperidin-1-yl-furan-2-carbaldehydeHCID 601613—
ProductHCID 11965417HCID 1196541730%

Reaction Steps

Through the procedure as employed in Production step 1, an amine moiety derived from piperidine (1.28 g) was introduced into 5-bromo-2-furaldehyde (875 mg), to thereby yield 5-piperidin-1-yl-furan-2-carbaldehyde (yield: 650 mg, 73%). The produced 5-piperidin-1-yl-furan-2-carbaldehyde (179 mg) was condensed with 3,4-dimethoxybenzyl cyanide (177 mg) through Method A (production step 2), to thereby yield the target product (yield: 100 mg, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697742B2
Source datasetuspto-grants-2014_04
ORD IDord-d4c3c99f1da04bc483d69d3a7a9dc4f8
Source noteuspto-grants-2014_04