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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742069Generated: October 30, 2026

4-Methylmorpholine → HCID 77709053, compound

https://huagongshe.com/reaction/742069

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantO-((4-Methoxyphenyl)methyl)hydroxylamineHCID 120426—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2(R)-[[4-methoxybenzenesulfonyl](3-picolyl)amino]-3-methyl-butanoic acid hydrochlorideHCID 70061703—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 77709053HCID 77709053—

Reaction Steps

2(R)-[[4-methoxybenzenesulfonyl](3-picolyl)amino]-3-methylbutanoic acid hydrochloride (2.41 g, 5.82 mmol), 1-hydroxybenzotriazole (0.786 g, 5.82 mmol), 4-methyl-morpholine (1.9 mL, 17.46 mmol), and O-(4-methoxybenzyl)hydroxylamine (1.78 g, 11.63 mmol) (prepared according to Pol. J. Chem. 55, 1163°-1167 (1981 )) are dissolved in methylene chloride (55 mL). N-[dimethylaminopropyl]-N'-ethylcarbodiimide hydrochloride (1.45 g, 7.57 mmol) is added, and the reaction is stirred overnight. The reaction is then diluted with water and extracted with methylene chloride. The combined organic extracts are washed with brine, dried (Na2SO4), and the solvent is evaporated. The crude product is purified by silica gel chromatography (ethyl acetate followed by 5% methanol/ethyl acetate) to give N-(4-methoxybenzyloxy)-2CR)-[[4-methoxybenzenesulfonyl]-(3-picolyl)amino]-3-methylbutanamide, m.p. 45°-53° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552419
Source datasetuspto-grants-1996_09
ORD IDord-6592f31eff1449adaeec501725b0437b
Source noteuspto-grants-1996_09