HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → HCID 70000822, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | L-Leucine, ethyl ester, hydrochloride (1:1) | HCID 11658447 | — |
| Reactant | HCID 18678400 | HCID 18678400 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70000822 | HCID 70000822 | 24.2% |
Reaction Steps
A solution of 4-(4-(dimethoxymethyl)piperidinyl)benzoic acid (0.450 g, 1.6 mmol), 1-(3-(dimethylamino)propyl)-3-ethylcarbodiimide HCl (0.340 g, 1.77 mmol), N-ethyl morpholine (0.50 mL, 3.9 mmol), hydroxybenzotriazole (0.239 g, 1.77 mmol), and L-leucine ethyl ester HCl (0.322 g, 1.8 mmol) in THF (15 mL) was stirred at ambient temperature overnight. The solvent was evaporated in vacuo and the residue was dissolved in methylene chloride. The organic phase was washed with 1N HCl, 1N NaOH, brine and dried (Na2SO4). The solvent was evaporated in vacuo and the residue purified by flash chromatography (methylene chloride-methanol, 19:1) to give 0.163 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506901B2 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-a14c6860aeef4d52897cee4e5711a41b |
| Source note | uspto-grants-2003_01 |