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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 269679생성일: 2026년 10월 25일

1,2-Dichloroethane → Benzyl{(1S)-4-[(tert-butoxycarbonyl)amino]-1-[({(4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentyl}amino)carbonyl]butyl}carbamate

https://huagongshe.com/reaction/269679

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Z-Ndelta-Boc-L-ornithineHCID 7350734—
반응물HCID 88986916HCID 88986916—
용매DimethylformamideHCID 6228—
생성물Benzyl{(1S)-4-[(tert-butoxycarbonyl)amino]-1-[({(4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentyl}amino)carbonyl]butyl}carbamateHCID 86625287—

반응 단계

Under argon, 0.155 g (0.42 mmol) of N2-[(benzyloxy)carbonyl]-N5-(tert-butoxycarbonyl)-L-ornithine and 0.12 g (0.55 mmol) of tert-butyl[(1S)-4-amino-1-(hydroxymethyl)butyl]carbamate (Example 247A) are dissolved in 6 ml of dimethylformamide. Then, at 0° C. (ice bath), 0.105 g (0.55 mmol) of EDC and 0.017 g (0.13 mmol) of HOBt are added. The mixture is slowly warmed to RT and stirred at RT for 12 h. The solution is concentrated in vacuo and the residue is taken up with ethyl acetate. The organic phase is washed successively with saturated sodium bicarbonate and sodium chloride solutions, dried over magnesium sulfate and evaporated in vacuo. The remaining solid is purified by preparative HPLC (Kromasil, mobile phase acetonitrile/0.25% aqueous trifluoroacetic acid 5:95→95:5).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07446102B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-b9091529bc9440bca5e74681b4ce68fc
출처 메모uspto-grants-2008_11