참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | (+-)-3-Quinuclidinol | HCID 15381 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-Azabicyclo[2.2.2]oct-3-yl methanesulfonate | HCID 416494 | 98% |
반응 단계
Quinuclidin-3-ol (10.0 g, 0.0787 mol) was dissolved under N2 in dry dichloromethane (200 ml) and cooled in an ice bath to 0° C. Methanesulphonyl chloride (7.3 ml, 10.8 g, 0.094 mol, 1.2 eq) and dry pyridine (7.64 ml, 7.46 g, 0.094 mol, 1.2 eq) were added and the mixture stirred at 0° C. for 20 min. The solution was then warmed to r.t. and stirred under N2 for 1 h. Saturated aqueous potassium carbonate solution (150 ml) was added, and the organic layer extracted and collected. The aqueous layer was re-extracted with EtOAc (3×200 ml), the organic solutions dried (Na2SO4), filtered, and evaporated to dryness under reduced pressure to yield a pale yellow oil which was pumped under high vacuum to remove any last traces of pyridine to yield the title compound (D8) (15.8 g, 98%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05981545 |
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| 출처 데이터셋 | uspto-grants-1999_11 |
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| ORD ID | ord-d15517aea070493592fcd55d6678db75 |
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| 출처 메모 | uspto-grants-1999_11 |
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