HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropyl iodide → (2R)-1-(tert-butoxycarbonyl)-4-isopropylpiperazine-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (2R)-1-(tert-Butoxycarbonyl)piperazine-2-carboxylic acid | HCID 24820285 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (2R)-1-(tert-butoxycarbonyl)-4-isopropylpiperazine-2-carboxylic acid | HCID 51440433 | — |
Reaction Steps
To (2R)-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid (4.5 g) and Na2CO3 (8.32 g) was added dry EtOH (135 ml) and isopropyl iodide (2.16 ml) and the mixture heated at reflux for 18 hours under argon. The solvent was then removed under reduced pressure, 5% MeOH/DCM (50 ml) added, the mixture stirred for 1 hour in a stoppered flask, filtered and washed through with DCM (2×10 ml). The filtrate was applied directly to a 120 g-silica Redisep® cartridge and purified using 10-70% MeOH/DCM. After evaporation, the product was isolated as a white foam (4.50 g), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943768B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-745b14d1a35b4bd4a6958f25120c87b3 |
| Source note | uspto-grants-2011_05 |