참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Malonate | HCID 7761 | — |
| 반응물 | Ethanol sodium ethoxide | HCID 23706232 | — |
| 반응물 | 1-Tert-butoxycarbonylpiperidin-4-yl benzenesulfonate | HCID 86619135 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Diethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)malonate | HCID 59605280 | — |
반응 단계
A mixture of 1-tert-butoxycarbonylpiperidin-4-ol, triethylamine, benzenesulfonyl chloride, and methylene chloride was stirred at ambient temperature for 2 days to yield 1-tert-butoxycarbonylpiperidin-4-yl benzenesulfonate. A mixture of 1-tert-butoxycarbonylpiperidin-4-yl benzenesulfonate obtained, diethyl malonate, 20% NaOEt-EtOH, and EtOH was heated under reflux with stirring for 22 hours to yield diethyl[1-(tert-butoxycarbonyl)piperidin-4-yl]malonate. A mixture of diethyl [1-(tert-butoxycarbonyl)piperidin-4-yl]malonate obtained, lithium borohydride, toluene, and THF was stirred at 60° C. for 18 hours to yield 2-(1-tert-butoxycarbonylpiperidin-4-yl)propane-1,3-diol, which was stirred together with 4M HCl-dioxane solution in MeOH at ambient temperature for 1 hour to yield 2-piperidin-4-ylpropane-1,3-diol hydrochloride.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07947690B2 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
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| ORD ID | ord-2ea39f6b43514390b30e9904b0204f6a |
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| 출처 메모 | uspto-grants-2011_05 |
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