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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 229828생성일: 2026년 10월 23일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → (2R,5S,6S)-5-((S)-2-tert-Butoxycarbonylamino-4-methyl-pentanoylamino)-6-hydroxy-2-methyl-azepane-1-carboxylic acid benzyl ester

https://huagongshe.com/ko/reaction/229828

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물DiisopropylethylamineHCID 81531—
반응물N-Boc-L-Leucine HydrateHCID 12373896—
반응물Racemic (2R,5S,6S)-5-Amino-6-hydroxy-2-methyl-azepane-1-carboxylic acid benzyl esterHCID 21036430—
반응물HCID 178418300HCID 178418300—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(2R,5S,6S)-5-((S)-2-tert-Butoxycarbonylamino-4-methyl-pentanoylamino)-6-hydroxy-2-methyl-azepane-1-carboxylic acid benzyl esterHCID 6900007277.8%

반응 단계

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide (0.164 g, 0.22 mmol) was added to a solution of Boc-Leucine-hydrate (0.190 g, 0.76 mmol), diisopropylethylamine (0.164 g, 0.22 ml, 1.27 mmol), hydroxybenztriazole (0.114 g, 0.83 mmol), and racemic (2R,5S,6S)-5-Amino-6-hydroxy-2-methyl-azepane-1-carboxylic acid benzyl ester (0.27 g, 0.57 mmol) in DMF (3.2 ml). The reaction was stirred overnight at RT, then was diluted with EtOAc (100 ml), washed with H2O (3×50 ml), brine (50 ml), dried with magnesium sulfate, filtered, concentrated in vacuo by rotary evaporation, and chromatographed (silica gel, 50% EtOAc/hexanes) to yield the title compound (0.218 g, 72%): 1H NMR: 7.40-7.29 (m, 5H), 6.75 (1H, bd), 5.12 (2H, AB), 5.0 (1H, bs), 4.15-3.72 (m, 2H), 3.06 (1H, d), 1.60-1.30 (m, 2H), 1.60-1.30 (m, 5H), 1.12 (3H, d), 0.97-0.87(6H, dd); Electrospray mass spec: M+H+=492.0

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07563784B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-0fdf3ab416f44090b08fe9c0481bf0cb
출처 메모uspto-grants-2009_07