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HRID 1444748作成日:2026年10月26日

2-Fluorobiphenyl-4-carboxaldehyde → 3-(3-((2-Fluorobiphenyl-4-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride

https://huagongshe.com/reaction/1444748

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluorobiphenyl-4-carboxaldehydeHCID 2759083—
反応物3-(5-Ammoniopentanoyl)pyridinium chlorideHCID 67337657—
触媒Hydrochloric AcidHCID 313—
溶媒EthanolHCID 702—
生成物3-(3-((2-Fluorobiphenyl-4-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochlorideHCID 6733915273.8%

反応条件

温度85 °C

反応手順

3-(5-Ammoniopentanoyl)pyridinium chloride (150 mg, 0.60 mmol) and 2-fluorobiphenyl-4-carboxaldehyde (155 mg, 0.78 mmol) were combined in a reaction vessel and treated with ethanol (10 mL) and concentrated HCl(aq) (5 drops). The vessel was then sealed and the reaction was heated to 85° C. overnight then cooled to room temperature. The reaction mixture was then concentrated under reduced pressure then partially dissolved into hot isopropanol. This mixture was left to cool and crystals formed. The crystals were recovered by vacuum filtration, washed with fresh isopropanol, and dried under vacuum giving 92 mg (36%) of a yellow solid. LC-MS: RT=5.88 min, [M+H]+=343.1.

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-7de7f797cb24449bbe4a42e5c238b9f8
出典メモuspto-grants-2010_02