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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727570Generated: November 1, 2026

4-Methylmorpholine → HCID 19705563, compound

https://huagongshe.com/reaction/727570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantBenzyloxyamine hydrochlorideHCID 102312—
ReactantHCID 19705446HCID 19705446—
SolventDichloromethaneHCID 6344—
ProductHCID 19705563HCID 19705563108.4%

Reaction Steps

A solution of α-[[[(4-methoxyphenyl)sulfonyl]amino]methyl]-3-(2-methylpropyl)-2-oxo-1-(2-phenylethyl)-3-pyrrolidineacetic acid (290 mg, 0.577 mmol) in dry CH2Cl2 (5 mL) is treated with CDI (112 mg, 0.692 mmol). Afar 1 h, 4-methylmorpholine (0.095 mL, 0.866 mmol) and O-benzylhydroxyamine HCl (138 mg, 0.866 mmol) are added. The solution is stirred at room temperature under N2 for 65 h. The solvent had evaporated, and the residual gel is diluted with EtOAc (25 mL). The solution is washed with 1N HCl (10 mL), 1N NaOH (10 mL), and brine (10 mL). The organic layer is dried over anhydrous MgSO4, filtered, and concentrated under reduced pressure to give 380 mg of an oil. The oil is purified by silica gel chromatography (30 g SG; 50% EtOAc/hexane) to provide 249 mg (71%) of the title compound as an oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712300
Source datasetuspto-grants-1998_01
ORD IDord-da6ea128228042ba96f6c07953ed8696
Source noteuspto-grants-1998_01