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HRID 1898935作成日:2026年10月27日

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

https://huagongshe.com/reaction/1898935

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物Ethyl 3,5-dihydroxynaphthalene-2-carboxylateHCID 14773083—
反応物3-NitrobenzylidenemalonitrileHCID 53825579—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
生成物ethyl 2-amino-3-cyano-9-hydroxy-4-(3-nitrophenyl)-4H-naphtho[1,2-b]pyran-8-carboxylateHCID 23369884—

反応手順

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.)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05571818
出典データセットuspto-grants-1996_11
ORD IDord-62e348a3c14447a6a7e9d31071cc2d75
出典メモuspto-grants-1996_11