HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → (+/-)-Methyl N,N'-dibenzyloxycarbonylpiperazine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Bis(benzyloxycarbonyl)piperazine-2-carboxylic acid | HCID 22632859 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (+/-)-Methyl N,N'-dibenzyloxycarbonylpiperazine-2-carboxylate | HCID 21847669 | — |
Reaction Steps
To a flask containing N,N'-dibenzyloxycarbonylpiperazine-2-carboxylic acid (Step 1, 12.83 g, 32.20 mmol) dissolved in dry DMF (50 mL) is added methyl iodide (5.6 mL, 90.00 mmol) and potassium carbonate (4.60 g, 32.20 mmol). The mixture is stirred for 4 hours at ambient temperature under an inert atmosphere. The reaction is concentrated in vacuo, diluted with ethyl acetate (150 mL), washed with water (3×50 mL) and saline, dried over MgSO4, concentrated in vacuo, and chromatographed on silica gel (70-230 mesh), eluting with hexane/ethyl acetate (50/50). The appropriate fractions are combined (Rf =0.55, TLC, hexane/ethyl acetate, 50/50) and concentrated in vacuo to give the title compound, NMR (CDCl3) 7.31, 5.15, 5.12, 4.70, 4.1-2.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05922707 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-a626d09972e949b49600f0b7114a58f7 |
| Source note | uspto-grants-1999_07 |