Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897952Generated: October 31, 2026

Ammonium Chloride → HCID 178513486, compound

https://huagongshe.com/reaction/1897952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178519569HCID 178519569—
ReactantHCID 178526939HCID 178526939—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductHCID 178513486HCID 178513486—

Reaction Steps

To a solution of 82.8 mg of 1-(3-chloro-2-fluorobenzoyl)-4-((6-(1H-pyrazol-3-ylamino)pyridin-2-yl)methyl)piperidine-4-carboxylic acid in 5 ml of chloroform were added 97 mg of ammonium chloride, 0.252 ml of triethylamine, 83 mg of hydroxybenzotriazole hydrate and 104 mg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride at room temperature, followed by stirring the reaction mixture at room temperature overnight. The reaction mixture was poured into saturated aqueous sodium bicarbonate solution, and extracted with ethyl acetate. The resulting ethyl acetate layer was dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated in vacuo. The resulting residue was purified by a preparative thin-layer chromatography (Kieselgel™ 60F254, Art5744 (Merck), chloroform/methanol=6/1) to give the title compound as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519136B2
Source datasetuspto-grants-2013_08
ORD IDord-3f22aaf9e782419f810554a4753061a8
Source noteuspto-grants-2013_08