Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 566771생성일: 2026년 10월 25일
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/566771
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| 반응물 | (2S)-2-Amino-3,3-dimethyl-1-butanol | HCID 2734079 | — |
| 반응물 | N-(1(S)-benzyl-2-methoxy-ethyl)-3(R)-(t-butoxycarbonylamino)succinamic acid benzyl ester | HCID 53930465 | — |
| 생성물 | 3(R)-(t-butoxycarbonylamino)-N-(1(S)-hydroxymethyl-2,2-dimethyl-propyl)succinamic acid benzyl ester | HCID 54052519 | 90% |
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 mmol) 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. 1H NMR (CDCl3): δ 7.22 (s, 5H), 6.52 (d, 1H, J=9.3 Hz), 5.62-5.52 (m, 1H), 5.25 (dd, 2H, J=12.1, 18.7 Hz), 4.58-4.48 (m, 1H), 3.90-3.78 (m, 2H), 3.58-3.50 (m, 1H), 3.22-3.10 (m, 1H), 2.78 (dd, 1H, J=5.9, 17.7 Hz), 2.52-2.45 (m, 1H), 1.22 (s, 9H), 0.98 (s, 9H). IR: 3322, 2960, 1730, 1664 1528, 1367, 1249, 1165, 1050 cm−1. Anal. Calculated for C22H34N2O6: C, 62.52, H, 8.12; N, 6.63. Found: C, 62.20; H, 8.13; N, 6.62.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06174915B1 |
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| 출처 데이터셋 | uspto-grants-2001_01 |
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| ORD ID | ord-f0f96ff13fc647419c8e4b0da6408ee4 |
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| 출처 메모 | uspto-grants-2001_01 |
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