HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 19969572, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | HCID 53837496 | HCID 53837496 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 19969572 | HCID 19969572 | 92.7% |
Reaction Steps
0.41 g of dicyclohexylcarbodiimide was added to 20 ml of a solution of 0.91 g of N-(N-benzyloxyleucyl)-α-[N-(3-methoxybenzyl)]carbamoylglycine and 0.23 g of N-hydroxysuccinimide in anhydrous dioxane. The mixture was stirred at room temperature for 16 hours. The reaction mixture was filtered to remove the insoluble materials. The filtrate was diluted with 50 ml of ethyl acetate. The resulting solution was washed with 1N hydrochloric acid and an aqueous solution saturated with sodium hydrogen carbonate, then dried with anhydrous magnesium sulfate, and subjected to distillation to remove the solvent, to obtain 0.81 g of 1-benzyloxy-6-isobutyl-3-[N-(3-methoxybenzyl)]carbamoylpiperazine-2,5-dione as a mixture of a cis form and a trans form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05607934 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-1fb1a42c7dda4fc79d6cbb5a423748d7 |
| Source note | uspto-grants-1997_03 |