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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72170생성일: 2026년 10월 24일

N-Carbobenzoxy-L-valine → ((R)-3-{(S)-2-[(S)-2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyrylamino)-3-methyl-butyrylamino]-3-methyl-butyrylamino}-2-hydroxy-propyl)-cyclohexylmethyl-phosphinic acid benzyl ester

https://huagongshe.com/ko/reaction/72170

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참여 물질

역할이름HCID투입량
반응물N-Carbobenzoxy-L-valineHCID 726987—
반응물{(R)-3-[(S)-2-((S)-2-tert-Butoxycarbonylamino-3-methyl-butyrylamino)-3-methyl-butyrylamino]-2-hydroxy-propyl}-cyclohexylmethyl-phosphinic acid benzyl esterHCID 68620254—
생성물((R)-3-{(S)-2-[(S)-2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyrylamino)-3-methyl-butyrylamino]-3-methyl-butyrylamino}-2-hydroxy-propyl)-cyclohexylmethyl-phosphinic acid benzyl esterHCID 68621798—

반응 단계

The resulting product from Step 1 was deprotected in a similar manner as Example 1, step 3, and the compound was used immediately and coupled to N-Cbz-L-valine in accordance with the procedures set forth in Example 12, Method B. The crude product was purified by gradient flash chromatography (methanol/methylene chloride) on a RediSep disposable column. 1H NMR (CD3Cl, 300 MHz): δ 7.45-7.25 (m, 10H), 6.0-5.85 (m, 1H), 5.18-4.92 (m, 4H), 4.50-4.33 (m, 2H), 4.31-4.04 (m, 2H), 3.43-3.26 (m, 2H), 2.25-2.03 (m, 3H), 2.02-1.70 (m, 8H), 1.37-1.10 (m, 4H), 1.04-0.82 (m, 20H). LCMS m/z: [M+H]+=757.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828974B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-66d0a3bbbf7847b5886cbbd27d02ae96
출처 메모uspto-grants-2014_09