Reaktion #41850
ord-42d126080e554dc4bcd910ea6e15d523
Reaktionsgleichung
Edukte
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturto warm to r.t.
- 2workup.STIRRINGagitated for 1.5 h
- 3FiltrationThe reaction mixture was filtered
- 4Einengenconcentrated
- 5workup.DISSOLUTIONThe resulting residue was dissolved in glacial acetic acid (60 mL)
- 6Temperaturheated to 100° C
- 7Temperaturthe resulting mixture heated at 100° C. for 1 h
- 8TrocknenThe organic layer was dried over sodium sulfate
- 9Einengenconcentrated
- 10workup.ADDITIONThe residue was treated with diethyl ether
- 11Filtrationthe resulting solid filtered
- 12Waschenwashed with diethyl ether
Vorschrift
(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-3-nitro-phenyl)-propionic acid methyl ester (16.8 mmol) and (R)-[4-(3,4-dichloro-benzyloxy)-phenyl]-hydroxy-acetic acid methyl ester (20.1 mmol) were dissolved in 80 mL of DCM, resin-bound triphenylphosphine (33.6 mmol) added and the mixture cooled to −20° C. To this solution was added DIAD (25.2 mmol) and the mixture was agitated for 30 min at −20° C. The mixture was slowly allowed to warm to r.t. and agitated for 1.5 h. The reaction mixture was filtered and concentrated. The resulting residue was dissolved in glacial acetic acid (60 mL) and heated to 100° C. Iron powder (336 mmol) was added and the resulting mixture heated at 100° C. for 1 h. The mixture was poured onto water and EtOAc. The mixture was brought to ˜pH 7 with sodium carbonate. The organic layer was dried over sodium sulfate and concentrated. The residue was treated with diethyl ether and the resulting solid filtered and washed with diethyl ether to provide (S)-2-tert-Butoxycarbonylamino-3-{(S)-2-[4-(3,4-dichloro-benzyloxy)-phenyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl}-propionic acid methyl ester (5.7 g). LC-MS (m/z) 502 (M-Boc).