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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053475Generated: October 30, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-[(2S,3S)-2-hydroxy-1-[N-[(3,4-methylenedioxy)phenyl]amino]-1-oxo-3-heptyl]-1-[N-(morpholine-4-carbonyl)amino]cyclohexanecarboxamide

https://huagongshe.com/reaction/2053475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-(Morpholine-4-carboxamido)cyclohexanecarboxylic acidHCID 11507137—
Reactant(2S,3S)-N-[(3,4-methylenedioxy)phenyl]-3-amino-2-hydroxyheptanamideHCID 59655569—
SolventDichloromethaneHCID 6344—
ProductN-[(2S,3S)-2-hydroxy-1-[N-[(3,4-methylenedioxy)phenyl]amino]-1-oxo-3-heptyl]-1-[N-(morpholine-4-carbonyl)amino]cyclohexanecarboxamideHCID 5363049590%

Reaction Steps

In anhydrous dichloromethane were dissolved 344 mg (1.23 mmol) of (2S,3S)-N-[(3,4-methylenedioxy)phenyl]-3-amino-2-hydroxyheptanamide, 315 mg (1.23 mmol) of 1-[N-(morpholine-4-carbonyl)amino]cyclohexanecarboxylic acid and 233 mg (1.48 mmol) of 1-hydroxybenzotriazole, and then, under nitrogen stream, 284 mg (1.48 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide was added to the above mixture at 0° C. Thereafter, the temperature of the reaction mixture was returned to room temperature, and the mixture was stirred overnight. The reaction mixture was concentrated under reduced pressure, the residue was dissolved in 80 ml of ethyl acetate, and the resulting mixture was washed successively with water, a 10% aqueous potassium hydrogen sulfate solution, a saturated aqueous sodium hydrogen carbonate solution and a saturated NaCl solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 574 mg (Yield: 90%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326799B2
Source datasetuspto-grants-2008_02
ORD IDord-93feae36715547a582445329b248a153
Source noteuspto-grants-2008_02