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HRID 454作成日:2026年10月24日

1,4-Dioxa-8-azaspiro(4.5)decane → 8-(5-Methoxypyridin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decane

https://huagongshe.com/ja/reaction/454

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
反応物3-Bromo-5-methoxypyridineHCID 817163—
試薬Sodium t-butoxideHCID 23676156—
触媒Palladium (II) acetateHCID 4144353—
触媒2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
溶媒TolueneHCID 1140—
生成物8-(5-Methoxypyridin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 6674228475.12%

反応条件

温度100 °C

反応手順

11/05 2011 07:58:54 +0200 A mixture of 3-bromo-5-methoxypyridine (1.5 g, 7.98 mmol), 1,4-dioxa-8-azaspiro[4.5]decane (1.023 ml, 7.98 mmol), palladium(II) acetate (0.107 g, 0.48 mmol) and dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (0.228 g, 0.48 mmol) in toluene (38.3 ml) and tBuOH (7.65 ml) was evacuated and flashed with N2 several times. Then sodium 2-methylpropan-2-olate (0.920 g, 9.57 mmol) was added and the reaction mixture was heated to 100°C for 2hrs. LCMS showed complete conversion. Reaction mixture had turned black. The reaction mixture was filtered through celite. The celite was washed with DCM. The combined filtrates were concentrated to yield 2.2g of brown oil, which starts to crystalise patially. Crude NMR showed only little unreacted amine (ca. 14%). The crude was purified by flash: The residue was purified by automated flash chromatography on a 100g column. A gradient from 40% to 100% of EA in Hep over 12CV, 100% EA over 6CV was used as mobile phase. The product was collected using the wavelength 254 nm. 1.5g of desired product were obtained as a light yellow oil.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-7ce32a5d4abb4826b07e10a8720e8cf8
出典メモ750 AstraZeneca ELN dataset