돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47731생성일: 2026년 10월 23일

tert-Butyl isothiocyanate → ethyl (2R)-6-{[(benzyloxy)carbonyl]amino}-2-{[(tert-butylamino)carbothioyl]amino}hexanoate

https://huagongshe.com/ko/reaction/47731

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl isothiocyanateHCID 11544—
반응물ethyl (2R)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoateHCID 86584429—
반응물HCID 178418790HCID 178418790—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
생성물ethyl (2R)-6-{[(benzyloxy)carbonyl]amino}-2-{[(tert-butylamino)carbothioyl]amino}hexanoateHCID 86584428—

반응 조건

온도80 °C

반응 단계

The process is performed as in Example 2, starting with 7.4 g of ethyl (2R)-2-amino-6-{[(benzyloxy)carbonyl]-amino}hexanoate with 5 cm3 of tert-butyl isothiocyanate in 200 cm3 of anhydrous ethanol at a temperature in the region of 20° C. for 20 hours. The reaction is completed by addition of a further 1 cm3 of isothiocyanate and heating for 2 hours at a temperature in the region of 80° C. The reaction medium is concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. The residue obtained is taken up in ether and concentrated again under the above conditions. 13 g of ethyl (2R)-6-{[(benzyloxy)carbonyl]amino}-2-{[(tert-butylamino)carbothioyl]amino}hexanoate are obtained in the form of a colorless oil. (αD20=−12.5±0.5 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-28959d29fab34f3faafa931b30da8b88
출처 메모uspto-grants-2004_03