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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629748Generated: November 2, 2026

Hydrochloric Acid → ((3S,6S)-6-((2-((S)-2-amino-3,3-bis(4-fluorophenyl)propanamido)-6-fluorophenoxy)methyl)morpholin-3-yl)methyl (2,2,2-trifluoroethyl)carbamate

https://huagongshe.com/reaction/629748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactanttert-butyl (2S,5S)-2-[(2-{[N-(tert-butoxycarbonyl)-4-fluoro-beta-(4-fluorophenyl)-L-phenylalanyl]amino}-6-fluorophenoxy)methyl]-5-[({[(2,2,2-trifluoroethyl)amino]carbonyl}oxy)methyl]morpholine-4-carboxylateHCID 86726347—
Solvent1,4-DioxaneHCID 31275—
Product((3S,6S)-6-((2-((S)-2-amino-3,3-bis(4-fluorophenyl)propanamido)-6-fluorophenoxy)methyl)morpholin-3-yl)methyl (2,2,2-trifluoroethyl)carbamateHCID 8657791296.2%

Reaction Steps

4M HCl (922 μl, 3.69 mmol) in dioxane was added to a solution of tert-butyl (2S,5S)-2-[(2-{[N-(tert-butoxycarbonyl)-4-fluoro-β-(4-fluorophenyl)-L-phenylalanyl]amino}-6-fluorophenoxy)methyl]-5-[({[(2,2,2-trifluoroethyl)amino]carbonyl}oxy)methyl]morpholine-4-carboxylate (310 mg, 0.369 mmol) in Dioxane (3.69 ml) at room temperature and the reaction stirred until complete by LC/MS (8 hrs). The solvent was removed in vacuo and ether was added to the residue. The desired product was filtered off to afford the title compound (253 mg, 0.355 mmol, 96% yield) as a white solid, MS (ESI): m/z=641.4 (M+H); 100% pure by LC/MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315475B2
Source datasetuspto-grants-2016_04
ORD IDord-a265d4bbd64b43098d5ec5e46f68cad7
Source noteuspto-grants-2016_04