참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Quinuclidinone | HCID 19507 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 반응물 | tert-butyl (2S)-2-amino-3-phenylpropanoate | HCID 6931633 | — |
| 반응물 | Pyridinium chloride | HCID 10176127 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 3-Quinuclidinol hydrochloride | HCID 2723725 | 74% |
반응 단계
To a solution of 9.00 g (56.25 mmol) 3-quinuclidinone and 4.15 g (18.75 mmol) Phe-O-t-Bu in 50 ml methanol was added over a 12 hour period a solution of 2.95 g (46.9 mmol) sodium cyanoborohydride in 13 ml methanol. After stirring for an additional 8 hours, 5.78 g (50.0 mmol) pyridine hydrochloride was added and after 11/2 hours stirring, sodium chloride was removed by filtration. The filtrate was concentrated to a foam which was treated with 15 ml methanol and 50 ml ethyl acetate to give a slurry of the byproduct 3-hydroxy quinuclidine hydrochloride (74% of excess) which was removed by filtration. The filtrate was concentrate to an oil and charged with 10 ml methanol to a 5×200 cm column of LH-20 and eluted with methanol. The product fraction contained 6.54 g of a mixture of diastereomers in a 55:45 ratio as established by HPLC.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05194605 |
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| 출처 데이터셋 | uspto-grants-1993_03 |
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| ORD ID | ord-bb5bf95155a544759cea26a6a40025e8 |
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| 출처 메모 | uspto-grants-1993_03 |
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