Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 370272생성일: 2026년 10월 25일
Cyclooctanecarbaldehyde → N-[9-(cyclooctylmethyl)-9-azabicyclo[3.3.1]nonan-3-yl]xanthene-9-carboxamide
https://huagongshe.com/reaction/370272
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyclooctanecarbaldehyde | HCID 81190 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | N-(9-azabicyclo[3.3.1]nonan-3-yl)xanthene-9-carboxamide hydrochloride | HCID 23283000 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | N-[9-(cyclooctylmethyl)-9-azabicyclo[3.3.1]nonan-3-yl]xanthene-9-carboxamide | HCID 15480669 | 19% |
반응 단계
38.5 mg of N-(9-azabicyclo[3.3.1]nonan-3-yl)xanthene-9-carboxamide hydrochloride and 44.1 mg of cyclooctanecarbaldehyde were suspended in 3 ml of methanol at room temperature, and 1.60 g of sodium triacetoxyborohydride was added thereto, followed by stirring for 12 hours at the same temperature. Saturated aqueous sodium bicarbonate was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by preparative thin layer chromatography (Kieselgel™60F254, Art5744 produced by Merck Co.: chloroform/methanol=19/1), and 9.0 mg of the title compound as a white solid was obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06140338 |
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| 출처 데이터셋 | uspto-grants-2000_10 |
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| ORD ID | ord-579a5cdcf625477db273cebaf834e15b |
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| 출처 메모 | uspto-grants-2000_10 |
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