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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 382158생성일: 2026년 10월 26일

Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → 3(R)-(t-butoxycarbonylamino)-N-(1(S)-hydroxymethyl-2,2-dimethyl-propyl)succinamic acid benzyl ester

https://huagongshe.com/reaction/382158

반응식

참여 물질

역할이름HCID투입량
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물(2S)-2-Amino-3,3-dimethyl-1-butanolHCID 2734079—
반응물N-(1(S)-benzyl-2-methoxy-ethyl)-3(R)-(t-butoxycarbonylamino)succinamic acid benzyl esterHCID 53930465—
생성물3(R)-(t-butoxycarbonylamino)-N-(1(S)-hydroxymethyl-2,2-dimethyl-propyl)succinamic acid benzyl esterHCID 5405251990%

반응 단계

As described in Example 1(f) for the preparation of N-(1(S)-benzyl-2-methoxyethyl)-3(R)-(t-butoxycarbonylamino)succinamic acid benzyl ester, N-t-butoxycarbonyl-D-aspartic acid β-benzyl ester (1.00 g, 3.10 mmol) and L-t-leucinol (400 mg, 3.40 mrnol) were coupled with BOP to afford 1.20 g (90%) of 3(R)-(t-butoxycarbonylamino)-N-(1(S)-hydroxymethyl-2,2-dimethyl-propyl)succinamic acid benzyl ester as a white powder, mp 186-7° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06306892B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-e446d43c98f048b9a762b118a2baadee
출처 메모uspto-grants-2001_10