반응 #71756
ord-c180fdccb7534d8fabcb7c4c30439f79
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상세 조건
See reaction.notes.procedure_details.
후처리
- 1농축The reaction solution was concentrated under reduced pressure
- 2workup.ADDITIONsaturated aqueous sodium bicarbonate solution was added
- 3추출followed by extraction with THF
- 4건조The organic layer was dried over anhydrous sodium sulfate
- 5농축concentrated under reduced pressure
- 6기타The resulting compound was used for the next reaction without purification
실험 절차
tert-Butyl cis(±)-4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidine-1-carboxylate obtained in Example (40a) (4.28 g, 11.7 mmol) was dissolved in methanol (20 mL). A 4 N hydrochloric acid/ethyl acetate solution (60 mL) was added, and the mixture was stirred at room temperature for 40 minutes. The reaction solution was concentrated under reduced pressure and then saturated aqueous sodium bicarbonate solution was added, followed by extraction with THF. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting compound was used for the next reaction without purification.