HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269685Generated: October 30, 2026
1,2-Dichloroethane → HCID 178453764, compound
https://huagongshe.com/reaction/269685
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | tert-butyl N-(3-amino-2-hydroxypropyl)carbamate | HCID 10511887 | — |
| Reactant | HCID 178454310 | HCID 178454310 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178453764 | HCID 178453764 | — |
Reaction Steps
Under argon, 0.30 g (0.49 mmol) of N2-[(benzyloxy)carbonyl]-N5-[[bis(tert-butoxycarbonyl)amino](imino)methyl]-L-ornithine-cyclohexanamine (1:1) and 0.12 g (0.64 mmol) of tert-butyl(3-amino-2-hydroxypropyl)carbamate 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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07446102B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-64dd89f955394c34bffe5b31649abdc7 |
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| Source note | uspto-grants-2008_11 |
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