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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1733653생성일: 2026년 10월 26일

Chloroform → Ethyl N-(1-((benzyloxy)carbonyl)-L-prolyl)-L-leucinate

https://huagongshe.com/reaction/1733653

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물Benzyloxycarbonyl-L-prolineHCID 101987—
반응물Ethyl 2-(p-toluenesulfonyloxyimino)-2-cyanoacetateHCID 2786718—
반응물L-Leucine, ethyl ester, hydrochloride (1:1)HCID 11658447—
용매TriethylamineHCID 8471—
생성물Ethyl N-(1-((benzyloxy)carbonyl)-L-prolyl)-L-leucinateHCID 64530754.1%

반응 단계

N-Benzyloxycarbonyl-L-proline (1.25 g) and L-leucine ethyl ester hydrochloride (1.0 g) are suspended into chloroform (10 ml), and therein is dissolved triethylamine (1.4 ml). To the solution is added ethyl 2-(p-toluenesulfonyloxyimino)-2-cyanoacetate (1.5 g) and the mixture is stirred at room temperature for 16 hours. After reaction, the reaction mixture is extracted with ethyl acetate. The exatract is washed with water, 1 N aqueous sodium hydrogen carbonate, water, 1 N hydrochloric acid and water in order and then dried over anhydrous magnesium sulfate. After drying, the solvent is distilled off and the residual oily substance (1.6 g) is dissolved in chloroform and then the mixture is subjected to a silica gel column chromatography (developer: chloroform). The first fraction thus obtained is concentrated and the resulting residue is crystallized from ether-petroleum ether to give N-(N-benzyloxycarbonyl-L-prolyl)-L-leucine ethyl ester (80 mg), melting point: 60°-64° C. The product is identified with an authentic sample by infrared spectrum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04242507
출처 데이터셋uspto-grants-1980_12
ORD IDord-b51b60f2a1244096b8d3f14c0d875741
출처 메모uspto-grants-1980_12