HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Phenylalanine, N-t-butyloxycarbonyl-4-nitro-, t-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-propionic acid | HCID 118071 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Phenylalanine, N-t-butyloxycarbonyl-4-nitro-, t-butyl ester | HCID 546503 | 97% |
Reaction Steps
To a mixture of the compound (6.9 g) obtained in Example 63 and methylene chloride (70 ml) were added t-butanol (20 ml), N,N-dimethylaminopyridine (2.63 g) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (4.9 g) and the resulting mixture was stirred at room temperature for 4 days. The reaction mixture was diluted with ethyl acetate and washed successively with 2 N HCl and a saturated aqueous sodium chloride solution; the organic layer was dried with anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent, n-hexane:ethyl acetate=3:1) to give 7.64 g of the titled compound (yield, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06534546B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-ff96db7c8e374413b724973db09f5f77 |
| Source note | uspto-grants-2003_03 |