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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908964Generated: October 25, 2026

4-Methylmorpholine → HCID 11517238, compound

https://huagongshe.com/reaction/908964

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantSodium HydroxideHCID 14798—
Reactant3-PhenylpropylamineHCID 16259—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-Dimethylamino-4-phenylcyclohexyl-acetic acid hydrochlorideHCID 67386131—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 11517238HCID 1151723858%

Reaction Steps

1-Hydroxybenzotriazole (273 mg, 2.0 mmol), 3-phenylpropylamine (0.142 ml, 1.0 mmol) and N-methylmorpholine (0.222 ml, 2.0 mmol) were added to a solution of (4-dimethylamino-4-phenylcyclohexyl)acetic acid hydrochloride (298 mg, 1.0 mmol) in dry dimethylformamide under argon. Dicyclohexylcarbodiimide (417 mg, 2.0 mmol) was added to the clear solution at 0° C. The reaction mixture was stirred at RT for 3 d, the urea which had precipitated out was filtered off with suction and the filtrate was introduced into a mixture of saturated NaCl solution (40 ml) and saturated NaHCO3 solution (10 ml). 5 M sodium hydroxide solution (12 ml, 60 mmol) was added to the aqueous phase and the mixture was diluted with water (300 ml) and stored at 5° C. for 3 d. The product was thereby produced as a colourless compound and was to be obtained in a yield of 58% (220 mg) by filtration, taking up of the residue in ethanol and concentration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017630B2
Source datasetuspto-grants-2011_09
ORD IDord-16d7fd7d4342463eb3f8fc47cc4dc58a
Source noteuspto-grants-2011_09