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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,4-Dioxa-8-azaspiro(4.5)decane | HCID 67435 | — |
| 반응물 | 3-Bromo-5-methoxypyridine | HCID 817163 | — |
| 시약 | Sodium t-butoxide | HCID 23676156 | — |
| 촉매 | Palladium (II) acetate | HCID 4144353 | — |
| 촉매 | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 8-(5-Methoxypyridin-3-yl)-1,4-dioxa-8-azaspiro[4.5]decane | HCID 66742284 | 75.12% |
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 데이터셋 | 750 AstraZeneca ELN dataset |
|---|
| ORD ID | ord-7ce32a5d4abb4826b07e10a8720e8cf8 |
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| 출처 메모 | 750 AstraZeneca ELN dataset |
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