참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Oxalyl chloride | HCID 65578 | — |
| 반응물 | 2-Furylglyoxylic acid | HCID 73846 | — |
| 반응물 | 3-Quinuclidinol, (-)- | HCID 91404 | — |
| 촉매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 2-fur-2-yl-2-oxoacetic acid (3R)-1-azabicyclo[2.2.2]oct-3-yl ester | HCID 66592053 | 52.8% |
반응 단계
Oxalyl chloride (9.75 ml, 0.112 mol) was added to a solution of oxofuran-2-ylacetic acid (10 g, 0.071 mol) and dimethylformamide (one drop) in 150 ml of chloroform (etanol free) at 0° C. The mixture was stirred and allowed to warm at room temperature. After five hours the solvent was evaporated. The residue was dissolved in chloroform and evaporated again. This procedure was repeated two times. The product obtained was disolved in CHCl3 (150 ml) and a solution of 3(R)-quinuclidinol (10.90 g, 0.086 mol) in CHCl3 (150 ml) was added to this at 0° C. The mixture was stirred and allowed to warm at room temperature. After 15 h at r.t., the mixture was washed with 10% aqueous potassium carbonate, then with water, dried over Na2SO4 and evaporated to give 9.34 g (52.5%) of the title compound as a dark oil. Estructure confirmed by NMR.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09333195B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-71edd0d99c004a4db45b9044c17fd79e |
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| 출처 메모 | uspto-grants-2016_05 |
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