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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
반응물3-Bromo-5-methoxypyridineHCID 817163—
시약Sodium t-butoxideHCID 23676156—
촉매Palladium (II) acetateHCID 4144353—
촉매2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
용매TolueneHCID 1140—
생성물8-(5-Methoxypyridin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 6674228475.12%

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-7ce32a5d4abb4826b07e10a8720e8cf8
출처 메모750 AstraZeneca ELN dataset