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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47732생성일: 2026년 10월 23일

Ethanol → ethyl (2R)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoate

https://huagongshe.com/ko/reaction/47732

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Thionyl ChlorideHCID 24386—
반응물H-D-Lys(Z)-OHHCID 1551330—
용매Ethyl AcetateHCID 8857—
생성물ethyl (2R)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoateHCID 86584429—

반응 조건

온도-25 °C

반응 단계

3.9 cm3 of thionyl chloride are added to a stirred suspension of 7.9 g of (2R)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoic acid (Nε-CBZ-D-lysine) in 120 cm3 of anhydrous ethanol cooled to a temperature in the region of −25° C. The mixture is stirred for 3 hours at this temperature and is then allowed to warm to about 20° C. After leaving for 3 days, the reaction mass is concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. The residue obtained is taken up in 200 cm3 of ethyl acetate and the resulting solution is washed with aqueous sodium carbonate solution and then with aqueous sodium chloride solution. The organic solution is dried over magnesium sulfate, filtered and concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. 7.4 g of ethyl (2R)-2-amino-6-{[(benzyloxy)-carbonyl]amino}hexanoate are obtained in the form of a pale yellow oil. (αD20=−11.7±0.6 at a concentration of 0.5% in methanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699895B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-805438be3a544e1ab8950860eaa8b951
출처 메모uspto-grants-2004_03