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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647712Generated: October 30, 2026

Piperidine → HCID 9863633, compound

https://huagongshe.com/reaction/1647712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantIsoquinolin-5-olHCID 30386—
Reactant[(3,4-Dimethoxyphenyl)methylidene]propanedinitrileHCID 219691—
SolventEthanolHCID 702—
ProductHCID 9863633HCID 9863633—

Reaction Steps

To a stirred suspension of 5-hydroxyisoquinoline (2.90 g) and 3,4-dimethoxy benzylidenemalononitrile (4.28 g) in ethanol (11 ml) was added dropwise piperidine (1.70 g). The suspension was then heated at reflux temperature for one hour forming a red solution. This was then allowed to cool to room temperature, depositing a brown solid. This was filtered off and washed with ethanol and ether and dried in vacuo at 60° C., yielding 2-amino-4-(3,4-dimethoxyphenyl)- 4H-pyrano[2,3-f] isoquinoline-3-carbonitrile as a yellow-brown solid, m.p. 225°-228° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434160
Source datasetuspto-grants-1995_07
ORD IDord-049a88eba40a43aca12f9e9b6421a261
Source noteuspto-grants-1995_07