Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630633Generated: October 30, 2026

(S)-benzyl 4-methyl-2-((S)-2-(2-morpholinoacetamido)-4-phenyl-N-((pivaloyloxy)methyl)butanamido)pentanoate → (S)-4-Methyl-2-((S)-2-(2-morpholinoacetamido)-4-phenyl-N-((pivaloyloxy)methyl)butanamido)pentanoic acid

https://huagongshe.com/reaction/630633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-benzyl 4-methyl-2-((S)-2-(2-morpholinoacetamido)-4-phenyl-N-((pivaloyloxy)methyl)butanamido)pentanoateHCID 86715394—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventMethanol--water (1/1)HCID 22242641—
Product(S)-4-Methyl-2-((S)-2-(2-morpholinoacetamido)-4-phenyl-N-((pivaloyloxy)methyl)butanamido)pentanoic acidHCID 8671539392.4%

Reaction Steps

Referring to FIG. 45, a slurry of Pd/C (10%) (200 mg) in MeOH/water (9:1) (10 mL) was added to a solution of (S)-benzyl 4-methyl-2-((S)-2-(2-morpholinoacetamido)-4-phenyl-N-((pivaloyloxy)methyl)butanamido)pentanoate (440 mg, 0.7 mmol) in MeOH (100 mL) and the suspension was stirred overnight under an atmosphere of hydrogen at RT. The reaction mixture was filtered over Celite, washed with MeOH and concentrated in vacuo to yield product (345 mg, 92%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315542B2
Source datasetuspto-grants-2016_04
ORD IDord-1fac1aff7a604d078446edb4f6adc527
Source noteuspto-grants-2016_04