HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269668Generated: October 26, 2026
1,2-Dichloroethane → HCID 86625285, compound
https://huagongshe.com/reaction/269668
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 57033312 | HCID 57033312 | — |
| Reactant | tert-Butyl {(4S)-5-amino-4-[(tert-butoxycarbonyl)amino]pentyl}carbamate | HCID 57440197 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86625285 | HCID 86625285 | — |
Reaction Steps
Under argon, 0.1 g (0.26 mmol) of (3S)-3-{[(benzyloxy)carbonyl]amino}-6-[(tert-butoxycarbonyl)amino]hexanoic acid (J. Med. Chem. (2002) 45:4246-4253) and 0.11 g (0.34 mmol) of tert-butyl{(4S)-5-amino-4-[(tert-butoxycarbonyl)amino]pentyl}carbamate (Example 86A) are dissolved in 6 ml of dimethylformamide. Then, at 0° C. (ice bath), 0.065 g (0.34 mmol) of EDC and 0.011 g (0.079 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 dried to constant weight under high vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07446102B2 |
|---|
| Source dataset | uspto-grants-2008_11 |
|---|
| ORD ID | ord-3160acda1df045e69d5a18b8e12955a8 |
|---|
| Source note | uspto-grants-2008_11 |
|---|