HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → N2-(tert-butoxycarbonyl)-3-hydroxy-N-(2,2,2-trifluoroethyl)-D-valinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 2,2,2-Trifluoroethylamine hydrochloride | HCID 9772 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-(tert-Butoxycarbonyl)-3-hydroxy-D-valine | HCID 11299247 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N2-(tert-butoxycarbonyl)-3-hydroxy-N-(2,2,2-trifluoroethyl)-D-valinamide | HCID 89495520 | — |
Reaction Steps
To a vial was added (R)—N-Boc-2-amino-3-hydroxy-3-methylbutanoic acid (CA, 500 mg, 2.144 mmol), 2,2,2-trifluoroethanamine hydrochloride (581 mg, 4.29 mmol), EDC (493 mg, 2.57 mmol), and HOBT (328 mg, 2.144 mmol). The reactants were dissolved in DCM (10 mL) and then DIEA (1.497 mL, 8.57 mmol) was added. The mixture was allowed to stir at RT overnight. The mixture was diluted with ethyl acetate, washed 2× with aqueous sodium hydrogen carbonate and 1× with brine. Aqueous layers were back extracted once with ethyl acetate, combined organic layers were dried with Na2SO4, filtered and the solvent was evaporated under reduced pressure. The material I-27a was used directly in the subsequent step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096598B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-fdc15f59045d4c0b85560e8fb6b3ce9e |
| Source note | uspto-grants-2015_08 |