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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369755Generated: October 31, 2026

Piperidine → HCID 23108312, compound

https://huagongshe.com/reaction/2369755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 61137645HCID 61137645—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 23108312HCID 23108312—

Reaction Conditions

Temperature50 °C

Reaction Steps

N-[2-(Acetylamino)propionyl]phenylalanine obtained in Experimental Example 21 (10 mg, 0.036 mmol) is suspended in N,N-dimethylformamide (5 ml), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (14 mg, 0.073 mmol), 1-hydroxybenzotriazole (15 mg, 0.11 mmol) and piperidine (40 μl, 0.40 mmol) are added to the suspension at room temperature, followed by stirring at 50° C. for 24 hours. To the reaction mixture is added water, and the resulting mixture is extracted three times with chloroform. The organic layer is washed with 10% hydrochloric acid and a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. After the solvent is distilled away under reduced pressure, the residue is purified by silica gel column chromatography to obtain 1-{(2-[N-(2-(acetylamino)propionyl)amino]-3-phenylpropionyl}piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08709752B2
Source datasetuspto-grants-2014_04
ORD IDord-f2d8da02e92f4bca9f13f09a48a5dfc3
Source noteuspto-grants-2014_04