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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374890Generated: October 31, 2026

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → 2-(5-chloro-3-pyridyloxy)-N-(2-methylpent-3-yn-2-yl)butyramide

https://huagongshe.com/reaction/1374890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant2-(5-Chloro-3-pyridyloxy)butyric acidHCID 21078378—
Reactant4-Aminomethyl-pent-2-yne hydrochlorideHCID 21078421—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product2-(5-chloro-3-pyridyloxy)-N-(2-methylpent-3-yn-2-yl)butyramideHCID 21078386—

Reaction Steps

To a stirred solution of 4-aminomethyl-pent-2-yne hydrochloride (2.67 g; prepared as described below) in dry N,N-dimethyl formamide (150 ml) at ambient temperature was added dry triethylamine (4.2 ml). The mixture was stirred at ambient temperature for 5 minutes and 1-hydroxybenzotriazole hydrate (2.97 g), N-(3-dimethylaminopropyl)-N′-ethyl carbodiimide hydrochloride (4.22 g) and 2-(5-chloro-3-pyridyloxy)butyric acid (4.53 g) were added sequentially. The mixture was stirred at ambient temperature for 2.75 hours, stored at ambient temperature for 18 hour and poured into water. The product was extracted into diethyl ether (three times) and the extracts were combined, washed with aqueous sodium o hydrogen carbonate (twice), water (twice) and dried over magnesium sulphate. The solvent was evaporated under reduced pressure and the residual gum fractionated by chromatography (silica: diethyl ether) to give a pale yellow oil, which was triturated with hexane to give the required product as a colourless solid, 4.5 g, m.p. 87–89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166621B2
Source datasetuspto-grants-2007_01
ORD IDord-ba3fb807c5c84802af8f07162190c794
Source noteuspto-grants-2007_01