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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899812Generated: October 27, 2026

Piperidine → ethyl 2-amino-3-cyano-9-hydroxy-4-(3-nitrophenyl)-4H-naphtho[1,2-b]pyran-8-carboxylate

https://huagongshe.com/reaction/1899812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantEthyl 3,5-dihydroxynaphthalene-2-carboxylateHCID 14773083—
Reactant3-NitrobenzylidenemalonitrileHCID 53825579—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Productethyl 2-amino-3-cyano-9-hydroxy-4-(3-nitrophenyl)-4H-naphtho[1,2-b]pyran-8-carboxylateHCID 23369884—

Reaction Steps

To a solution of ethyl 3,5-dihydroxynaphthalene-2-carboxylate (4.5 g) in ethanol (40 ml) was added 3-nitrobenzylidenemalonitrile (3.9 g) and piperidine (1.95 ml). The mixture was heated under reflux for 15 minutes whereupon a yellow precipitate was observed to form. The mixture was allowed to cool to room temperature, diluted with ether (100 ml) and the solid filtered off to yield ethyl 2-amino-3-cyano-9-hydroxy-4-(3-nitrophenyl)-4H-naphtho[1,2-b]pyran-8-carboxylate as a yellow powder, m.p. 260°-261° C. (dec.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574034
Source datasetuspto-grants-1996_11
ORD IDord-eeee3881b99e4e86b2bcc1aef1394c96
Source noteuspto-grants-1996_11