HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 23533837, compound → HCID 12148457, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 23533837 | HCID 23533837 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 12148457 | HCID 12148457 | — |
Reaction Steps
N-[2-[3-(allyloxycarbonyl)-benzyloxy]-1(S)-cyanoethyl]-3-methyl-Nα-(t-butoxycarbonyl)-L-phenylalaninamide (4.36 g, 8.37 mmol) in formic acid (47 mL) is stirred at room temp. for 6 h, after which time the formic acid is evaporated at 25° C. The residue is then dissolved in water (50 mL), basified with sat'd aqueous NaHCO3, and extracted with ethyl acetate (3×50 mL). The combined organic layers are then washed with water (50 mL), brine (50 mL), dried (MgSO4) and evaporated to yield N-[2-[3-(allyloxycarbonyl)-benzyloxy]-1(S)-cyanoethyl]-3-methyl-L-phenylalaninamide, as a clear oil, which is utilized without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06812237B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-eaeaa65bdc084c3b9cb1a8ba9c6f6b93 |
| Source note | uspto-grants-2004_11 |