Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethyl Acetate → 1-cyclopentyl N-[1-(tert-butoxycarbonyl)pyrrolidin-3-yl]-L-leucinate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Tert-butyl 3-oxopyrrolidine-1-carboxylate | HCID 471360 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | L-leucine cyclopentyl ester tosylate | HCID 86633653 | — |
| 용매 | 1,1-Dichloroethane | HCID 6365 | — |
| 생성물 | 1-cyclopentyl N-[1-(tert-butoxycarbonyl)pyrrolidin-3-yl]-L-leucinate | HCID 86686416 | — |
반응 단계
To a solution of N-tert-butoxycarbonyl-3-pyrrolidinone (0.382 g, 4.76 mmol) in dichloroethane (20 mL) was added L-leucine cyclopentyl ester tosylate (1.96 g, 5.3 mmol) and sodium triacetoxyborohydride (2.65 g, 12.5 mmol). The mixture was stirred at room temperature for 3 hours, then poured into ethyl acetate (150 mL) and quenched with saturated ammonium chloride solution (50 mL) and washed with saturated sodium hydrogen carbonate solution (3 times 30 mL). The organic extracts were dried (MgSO4), concentrated and purified by flash column chromatography (7:3 ethyl acetate:heptane) to yield the desired product. LC/MS: m/z 369.25 [M+H]+
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09321718B2 |
| 출처 데이터셋 | uspto-grants-2016_04 |
| ORD ID | ord-6da453aad4f84aac847932ee8559d33c |
| 출처 메모 | uspto-grants-2016_04 |