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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988273Generated: November 4, 2026

Sodium Hydroxide → 2-((2-tertbutoxycarbonylamino-3-(4-fluorophenyl)propionyl)-N-methylamino)-3-methylbutyric acid 2-(3-t-butyl-4-hydroxyphenyl)-1-(1,2,4-oxadiazol-5-yl)ethylamide

https://huagongshe.com/reaction/1988273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantDimethylacetamideHCID 31374—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantBoc-Phe(4-F)-N-Me-Val-Tyr(3-tBu)-NH2HCID 131727517—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
SolventAcetic acid--water (1/1)HCID 21899381—
Product2-((2-tertbutoxycarbonylamino-3-(4-fluorophenyl)propionyl)-N-methylamino)-3-methylbutyric acid 2-(3-t-butyl-4-hydroxyphenyl)-1-(1,2,4-oxadiazol-5-yl)ethylamideHCID 8676090276%

Reaction Steps

A solution of Boc-Phe(4-F)-N-Me-Val-Tyr(3-tBu)-NH2 (600 mg, 0.976 mmol) and N,N-dimethylacetamide (0.2 ml, 1.5 mmol) in dioxane (3 ml) was stirred at room temperature for 1 hour and mixed with a solution of sodium hydroxide (108 mg) and hydroxyamine hydrochloride (190 mg) in acetic acid/water (7 ml/3 ml). The mixture was stirred at room temperature for 10 min., mixed with water and filtered; a solution of the thus obtained precipitate in acetic acid/dioxane (10 ml/10 ml) was stirred at 60° C. overnight. The reaction mixture was mixed with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and evaporated to remove the solvent under reduced pressure; the thus obtained residue was subjected to silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:1), giving the titled compound (474 mg, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553969B1
Source datasetuspto-grants-2009_06
ORD IDord-2902be423cab4031a273ffe85431ba25
Source noteuspto-grants-2009_06