HuagongsheHuagongshe Chemistry Print Report · For research reference only
Palmitoyl chloride → (R)-tert-butyl 3-((R)-2,3-bis(decylcarbamoyloxy)propylthio)-2-palmitamidopropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Palmitoyl chloride | HCID 8206 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (R)-tert-butyl 2-amino-3-((R)-2,3-bis(decylcarbamoyloxy)propylthio)propanoate | HCID 86678326 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-tert-butyl 3-((R)-2,3-bis(decylcarbamoyloxy)propylthio)-2-palmitamidopropanoate | HCID 86678327 | — |
Reaction Steps
To a solution of (R)-tert-butyl 2-amino-3-((R)-2,3-bis(decylcarbamoyloxy)propylthio)propanoate in dry DCM (0.1 M) at 0° C. was added DIEA (1.2 eq) and palmitoyl chloride (1.1 eq). The reaction was allowed to warm to room temperature then stirred for 16 hours. The crude reaction was then concentrated and purified by flash chromatography on a COMBIFLASH® system (ISCO) using a gradient 0-60% EtOAc/Hex to afford the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365506B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-f61b9a51991d444ab9d1fb5f590e045d |
| Source note | uspto-grants-2016_06 |