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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474149Generated: November 1, 2026

2-Iodoxybenzoic acid → (2R)-1-benzyl-N-(4-(ethoxyamino)-3,4-dioxo-1-phenylbutan-2-yl)-5-oxopyrrolidine-2-carboxamide

https://huagongshe.com/reaction/1474149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Iodoxybenzoic acidHCID 108794—
ReactantSodium BicarbonateHCID 516892—
Reactant(2R)-1-benzyl-N-(4-(ethoxyamino)-3-hydroxy-4-oxo-1-phenylbutan-2-yl)-5-oxopyrrolidine-2-carboxamideHCID 86652462—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(2R)-1-benzyl-N-(4-(ethoxyamino)-3,4-dioxo-1-phenylbutan-2-yl)-5-oxopyrrolidine-2-carboxamideHCID 532575483.02%

Reaction Steps

IBX (2-iodoxybenzoic acid 432 mg, 0.694 mmol) was added to a solution of (2R)-1-benzyl-N-(4-(ethoxyamino)-3-hydroxy-4-oxo-1-phenylbutan-2-yl)-5-oxopyrrolidine-2-carboxamide (218 mg, 0.496 mmol) in DMSO (2 ml). After stirring for 2 h at room temperature more IBX (123 mg, 0.198 mmol) was added and the stirring was continued overnight. Saturated aqueous NaHCO3 solution was added and the reaction mixture was diluted with water and dichloromethane. The precipitate formed was filtered off, the organic layer was separated and the aqueous layer extracted with dichloromethane. The combined organic layers were washed with water and dried (MgSO4). The solvent was removed in vacuo, the resulting residue was redissolved in a small amount of dichloromethane and diethylether was added. The white precipitate formed was filtered, washed with diethylether and dried in vacuo. The crude product was dissolved in dichloromethane and treated with three drops of aqueous HCl (4M in dioxane). Removal of the solvent provided the title compound (8.2 mg, 0.015 mmol, 3.02% yield). ESI-MS [M+H]+=438.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018206B2
Source datasetuspto-grants-2015_04
ORD IDord-d20bcb500b2746b5b13e86056b0f1d0e
Source noteuspto-grants-2015_04