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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220542Generated: November 1, 2026

Triethylamine → N-(2-{4-[3'-(4-Fluoro-phenyl)-2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-ylmethyl]-pyrazol-1-yl}-ethyl)-N-methyl-methanesulfonamide hydrochloride

https://huagongshe.com/reaction/220542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 59321877HCID 59321877—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductN-(2-{4-[3'-(4-Fluoro-phenyl)-2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-ylmethyl]-pyrazol-1-yl}-ethyl)-N-methyl-methanesulfonamide hydrochlorideHCID 6859621497%

Reaction Steps

Dissolve (2-{4-[3′-(4-fluoro-phenyl)-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-ylmethyl]-pyrazol-1-yl}-ethyl)-methyl-amine (0.124 g, 0.314 mmol) in DCM (3 mL) with triethylamine (66 μL, 0.470 mmol). Add methanesulfonyl chloride (26 μL, 0.329 mmol) dropwise in DCM (1 mL). Stir the mixture for 20 hr. Dilute with saturated aqueous sodium bicarbonate then extract 3 times with DCM. Dry (sodium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 4.5:95.5 2 M ammonia in methanol:DCM), to give a yellow oil. Dissolve the oil in methanol and add ammonium chloride then sonicate the mixture for 10 min. Evaporate the solution to give the title compound as a yellow solid (0.154 g, 97%). MS (ES): m/z=474 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-0b1465dc6009492884cef2e16580b014
Source noteuspto-grants-2012_06