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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900631Generated: October 31, 2026

4-Methylmorpholine → N-(3-methyl-2(S)-(t-butoxycarbonylamino)but-1-yl)phenylalanylmethionine-methyl ester

https://huagongshe.com/reaction/1900631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantL-Methionine, methyl ester, hydrochlorideHCID 11435579—
ReactantN-(3-methyl-2(S)-(t-butoxycarbonylamino)but-1-yl)phenylalanineHCID 22846563—
SolventDimethylformamideHCID 6228—
ProductN-(3-methyl-2(S)-(t-butoxycarbonylamino)but-1-yl)phenylalanylmethionine-methyl esterHCID 2286701479.5%

Reaction Steps

N-Methyl morpholine (4.0 ml) and 1-ethyl-3-(3-dimethylaminopropyl) carbodimide (EDC) hydrochloride (0.96 g, 0.005 mole) were added to a solution of the product of Step B (1.76 g, 0.005 mole), methionine methyl ester hydrochloride (1.0 g, 0.005 mole) and 1-hydroxybenzotriazole hydrate (HOBT,0.677 g, 0.005 mole) in dimethylformamide (DMF, 30 ml) the reaction mixture was stirred at room temperature over the weekend, concentrated in vacuo and taken up in ice, water, and ethyl acetate. After addition of 10% aqueous citric acid, the ethyl acetate solution was separated, washed with water (2×), aqueous NaHCO3 and brine, and dried over sodium sulfate. Filtration and evaporation of the ethyl acetate solution gave a pale yellow residue, which was purified by column chromatography (silica gel) using 35% ethyl acetate-hexane. The title compound (1.97 g) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576293
Source datasetuspto-grants-1996_11
ORD IDord-5b00b4f4b29647cda6736e1a12a62473
Source noteuspto-grants-1996_11