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HRID 1444749作成日:2026年10月24日

6-Phenoxynicotinaldehyde → 2-phenoxy-5-((2-(pyridin-3-yl)-5,6-dihydropyridin-3(4H)-ylidene)methyl)pyridine dihydrochloride

https://huagongshe.com/ja/reaction/1444749

反応式

関与物質

役割名称HCID仕込み量
反応物6-PhenoxynicotinaldehydeHCID 2776500—
反応物3-(5-Ammoniopentanoyl)pyridinium chlorideHCID 67337657—
溶媒IsopropanolHCID 3776—
生成物2-phenoxy-5-((2-(pyridin-3-yl)-5,6-dihydropyridin-3(4H)-ylidene)methyl)pyridine dihydrochlorideHCID 67337936147.2%

反応条件

温度80 °C

反応手順

3-(5-Ammoniopentanoyl)pyridinium chloride (101 mg, 0.40 mmol) and 6-phenoxynicotinaldehyde (120 mg, 0.60 mmol) were combined in a reaction vessel and treated with isopropanol (15 mL). The reaction vessel was sealed and the reaction was heated to 80° C. with stirring overnight. The reaction was then cooled to room temperature. The precipitate that formed was recovered by vacuum filtration and washed with a 20% solution of isopropanol in hexane and then with ether. The recovered solid was then dried under vacuum giving 122 mg (73%) of a pale yellow solid. LC-MS: RT=5.08 min, [M+H]+=342.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07662965B2
出典データセットuspto-grants-2010_02
ORD IDord-ae0f567c7dfb4e0f9b94302d12f9c479
出典メモuspto-grants-2010_02