Ethanol → (2R,4R)-4-amino-5-biphenyl-4-yl-2-hydroxypentanoic acid ethyl ester

(3R,5R)-5-Biphenyl-4-ylmethyl-1-(2,2-dimethylpropionyl)-3-hydroxypyrrolidin-2-one (56 g, 0.156 mol) was dissolved in EtOH (700 mL) and 12N HCl (700 mL). The mixture was heated to 90-95° C. for 20 hours. The mixture was concentrated on an 80° C. water bath under reduced pressure. EtOH (100 mL) was added to the residue, and the resulting mixture was filtered to yield a yellow solid. This solid was suspended in 3N HCl/EtOH (800 mL). The mixture was refluxed for 3 hours. The solution was concentrated to a reduced volume (˜200 mL volume), and ether (200 mL) was added. The resulting slightly yellow solid was filtered and dried under reduced pressure to yield (2R,4R)-4-amino-5-biphenyl-4-yl-2-hydroxypentanoic acid ethyl ester (43 g).

1. concentrationThe mixture was concentrated on an 80° C. water bath under reduced pressure
2. additionEtOH (100 mL) was added to the residue
3. filtrationthe resulting mixture was filtered
4. customto yield a yellow solid
5. temperatureThe mixture was refluxed for 3 hours
6. concentrationThe solution was concentrated to a reduced volume (˜200 mL volume), and ether (200 mL)
7. additionwas added
8. filtrationThe resulting slightly yellow solid was filtered
9. customdried under reduced pressure

ORD 기록

ord-86a56dd68eb74788a355cd6967c24cfc

출처 데이터셋

uspto-grants-2016_07

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US09388145B2