HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → HCID 18603232, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Glycinamide hydrochloride | HCID 2723639 | — |
| Reactant | BOC-D-LEU-OH H2O | HCID 2724763 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 18603232 | HCID 18603232 | — |
Reaction Steps
1.55 g (0.014 mole) of glycinamide hydrochloride is dissolved in 50 ml of DMF by warming to 50°. The solution is cooled to 25° and 2 ml of triethylamine is added, followed by 1.89 g of hydroxybenztriazole, 3.5 g (0.014 mol) of BOC-D-leucine H2O and lastly, 2.9 g (0.014 mol) of dicyclohexylcarbodiimide. The mixture is stirred two days at 25° and then evaporated in vacuo to an oil. The oil is dissolved in 200 ml EtOAC, 50 ml CHCl3. The organic solution is washed with water, 20% citric acid solution, water, 10% Na2CO3 solution. The EtOAc solution is dried over MgSO4 and the solvent removed in vacuo to a glass, 3.7 g (93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04596819 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-b1cf025d323e486bac7fa0720522d659 |
| Source note | uspto-grants-1986_06 |