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HRID 1824503作成日:2026年10月27日

Piperidine → 7-Methyl-2-[2-methyl-4-(3-piperidin-1-yl-propoxy)-phenyl]-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1824503

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物2-(4'-Chloropropoxy-2'-methylphenyl)-7-methylimidazo[1,2-a]pyridineHCID 22015639—
生成物7-Methyl-2-[2-methyl-4-(3-piperidin-1-yl-propoxy)-phenyl]-imidazo[1,2-a]pyridineHCID 10270093—

反応手順

The product of Step C (200 mg) and piperidine (2.0 mL) were heated at 100° C. for 2.5 hours. The reaction was cooled to ambient temperature and partitioned between ethyl acetate (10 mL) and saturated sodium bicarbonate solution (10 mL). The aqueous portion was extracted with additional ethyl acetate (10 mL) and the organic portions combined, washed with brine, and evaporated. The residue was purified via silica gel chromatography (dichloromethane/methanol) to give the title compound (110 mg). 1H-NMR (CD3OD) δ 8.28 (d, J=7.0 Hz, 1H), 7.78 (s, 1H), 7.61 (d, J=8.0 Hz, 1H), 7.31 (s, 1H), 6.84 (s, 1H), 6.79 (m, 2H), 4.04 (t, J=6.0 Hz, 2H), 2.50 (m, 12H), 1.99 (m, 2H), 1.64 (m, 4H), 1.51 (m, 2H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07041827B2
出典データセットuspto-grants-2006_05
ORD IDord-6811eba86ee7493b8f20952ca6725102
出典メモuspto-grants-2006_05