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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1180753생성일: 2026년 10월 25일

HCID 58979703, 화합물 → HCID 58979660, 화합물

https://huagongshe.com/reaction/1180753

반응식

참여 물질

역할이름HCID투입량
반응물HCID 58979703HCID 58979703—
반응물(1-Benzylcyclohexyl)methanolHCID 58979707—
반응물HCID 69202106HCID 69202106—
반응물N-((5S)-5-amino-6-hydroxy-7-oxo-7-{[(1R)-1-phenylethyl]amino}heptyl)-4-morpholinecarboxamide hydrochlorideHCID 69236903—
생성물HCID 58979660HCID 58979660—

반응 단계

[1-(2,6-Difluorobenzyl)cyclobutyl]methyl(1S)-1-(1-hydroxy-2-oxo-2-{[(1R)-1-phenylethyl]amino}ethyl)-5-{[(methylamino)carbonyl]amino}pentylcarbamate was prepared as in example 9i except that [1-(2,6-difluorobenzyl)cyclobutyl]methanol was substituted for (1-benzylcyclohexyl)methanol, and (3S)-3-amino-2-hydroxy-7-{[(methylamino)carbonyl]amino}-N-[(1R)-1-phenylethyl]heptanamide hydrochloride was substituted for N-((5S)-5-amino-6-hydroxy-7-oxo-7-{[(1R)-1-phenylethyl]amino}heptyl)-4-morpholinecarboxamide hydrochloride. 1H NMR (300 MHz, DMSO-d6) δ 8.06 (m, 1H), 7.01-7.45 (m, 8H), 6.43 (d, J=8 Hz, 1H), 5.83 (m, 1H), 5.60 (m, 2H), 4.94 (m, 1H), 3.70-4.00 (m, 4H), 3.35 under water peak (m, 3H), 2.65-3.00 (m, 4H), 1.60-1.85 (m, 6H), 1.10-1.50 (m, 9H). ES-LCMS m/z 573 (M−H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07282512B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-1cb28f65428a4a71ae33e4b3eea0301a
출처 메모uspto-grants-2007_10