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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | tert-Butyl isothiocyanate | HCID 11544 | — |
| 반응물 | ethyl (2R)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoate | HCID 86584429 | — |
| 반응물 | HCID 178418790 | HCID 178418790 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | ethyl (2R)-6-{[(benzyloxy)carbonyl]amino}-2-{[(tert-butylamino)carbothioyl]amino}hexanoate | HCID 86584428 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06699895B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-28959d29fab34f3faafa931b30da8b88 |
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| 출처 메모 | uspto-grants-2004_03 |
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