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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251809Generated: October 31, 2026

Triethylamine → HCID 69147108, compound

https://huagongshe.com/reaction/2251809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Propan-2-yl)benzene-1-sulfonyl chlorideHCID 2734882—
ReactantHCID 69145023HCID 69145023—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69147108HCID 69147108—

Reaction Conditions

Temperature45 °C

Reaction Steps

520 mg (2.38 mmol) of 5-(4-allylpiperazin-1-yl)pyridin-2-ylamine and 495 mg (2.26 mmol) of 4-isopropylbenzenesulfonyl chloride were dissolved in 5 ml of tetrahydrofuran at room temperature, after which 1.0 ml (7.15 mmol) of triethylamine was added dropwise and the mixture was stirred at 40-50° C. for 6 hours. After the solvent had been evaporated down to dryness, the resulting residue was treated with water and this mixture was made acid using 1N aqueous hydrochloric acid and extracted twice with diethyl ether. The aqueous phase was made alkaline, to pH 9-10, using a 1N aqueous solution of sodium hydroxide and then extracted twice with ethyl acetate. After the combined organic phases had been dried over sodium sulfate, the drying agent had been filtered off and the solvent had been evaporated down to dryness, the resulting residue was chromatographed on silica gel using ethyl acetate. After the solvent had been removed, the resulting residue was brought into solution using a little diethyl ether in dichloromethane and then converted into the hydrochloride using ethereal hydrochloric acid. 415 mg (44% of theory) of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320979B2
Source datasetuspto-grants-2008_01
ORD IDord-56bbf5418d0d440eaadc8d2745c543c7
Source noteuspto-grants-2008_01