Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 451767생성일: 2026년 10월 26일
(S)-2-(Boc-amino)-3-cyclohexyl-N-methoxy-N-methylpropanamide → (S)-tert-butyl 1-cyclohexyl-3-oxopentan-2-ylcarbamate
https://huagongshe.com/reaction/451767
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | (S)-2-(Boc-amino)-3-cyclohexyl-N-methoxy-N-methylpropanamide | HCID 10495486 | — |
| 반응물 | HCID 178461630 | HCID 178461630 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | (S)-tert-butyl 1-cyclohexyl-3-oxopentan-2-ylcarbamate | HCID 15730499 | — |
반응 단계
To a solution of (S)-tert-butyl 3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate (5.23 g, 16.66 mmol) in anhydrous toluene (80 mL) at −20° C. was added EtMgBr (3 M in Et2O, 16.7 mL, 49.97 mmol) slowly. The reaction was allowed to warm to 0° C., and stirred at this temperature for 2 h. The reaction was quenched with 1 M HCl at 0° C. and extracted with EtOAc. The organic phase was washed with sat. aq. NaHCO3, brine, concentrated to give (S)-tert-butyl 1-cyclohexyl-3-oxopentan-2-ylcarbamate. The product was used in the next step without further purification. MS ESI +ve m/z 306 (M+Na).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08487108B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-56ff7388ade14b54ab8a34209b8ef806 |
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| 출처 메모 | uspto-grants-2013_07 |
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