HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 269681Erstellt: 25. Oktober 2026
1,2-Dichloroethane → Benzyl[(1S)-4-[(tert-butoxycarbonyl)amino]-1-({[(1S)-2-[(tert-butoxycarbonyl)amino]-1-(hydroxymethyl)ethyl]amino}carbonyl)butyl]carbamate
https://huagongshe.com/reaction/269681
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dichloroethane | HCID 11 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | Z-Ndelta-Boc-L-ornithine | HCID 7350734 | — |
| Edukt | (S)-tert-Butyl (2-amino-3-hydroxypropyl)carbamate | HCID 10702853 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Benzyl[(1S)-4-[(tert-butoxycarbonyl)amino]-1-({[(1S)-2-[(tert-butoxycarbonyl)amino]-1-(hydroxymethyl)ethyl]amino}carbonyl)butyl]carbamate | HCID 131727171 | — |
Reaktionsschritte
Under argon, 0.18 g (0.49 mmol) of N2-[(benzyloxy)carbonyl]-N5-(tert-butoxycarbonyl)-L-ornithine and 0.122 g (0.64 mmol) of tert-butyl[(2S)-2-amino-3-hydroxypropyl]carbamate (Example 251A) are dissolved in 6 ml of dimethylformamide. Then, at 0° C. (ice bath), 0.123 g (0.64 mmol) of EDC and 0.02 g (0.15 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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07446102B2 |
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| Quelldatensatz | uspto-grants-2008_11 |
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| ORD ID | ord-1f59c99da0cc4338b9685ed6e7930911 |
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| Quellennotiz | uspto-grants-2008_11 |
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