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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727531Generated: November 1, 2026

4-Methylmorpholine → N-Benzyloxy-alpha-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl]-3-(2-methylpropyl)-2-oxo-1-(2-phenylethyl)-3-pyrrolidineacetamide

https://huagongshe.com/reaction/727531

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantBenzyloxyamine hydrochlorideHCID 102312—
Reactantalpha-[2-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl]-3-(2-methylpropyl)-2-oxo-1-(2-phenylethyl)-3-pyrrolidineacetic AcidHCID 19705466—
SolventDichloromethaneHCID 6344—
ProductN-Benzyloxy-alpha-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl]-3-(2-methylpropyl)-2-oxo-1-(2-phenylethyl)-3-pyrrolidineacetamideHCID 1970547249%

Reaction Steps

CDI (82 mg, 0.51 mmol) is added to a solution of α-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl]-3-(2-methylpropyl)-2-oxo-1-(2-phenylethyl)-3-pyrrolidineacetic acid (202 mg, 0.424 mmol) and CH2Cl2 (3.2 mL) at room temperature, and the solution is stirred for 1 hour at room temperature. O-Benzylhydroxylamine hydrochloride (98 mg, 0.614 mmol) and 4-methylmorpholine (84 uL, 0.76 mmol) are added in succession, and the solution is allowed to stir overnight at room temperature. Aqueous workup (CH2Cl2, MgSO4) and purification by column chromatography (2% acetene/CH2Cl2) gives 120 mg (49%) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712300
Source datasetuspto-grants-1998_01
ORD IDord-37b3c58edb8f4f1584a4cab4acec1a1b
Source noteuspto-grants-1998_01