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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403618Generated: October 30, 2026

Diisopropylethylamine → HCID 70664906, compound

https://huagongshe.com/reaction/1403618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1',2',3',6'-Tetrahydro-2,4'-bipyridineHCID 15166842—
ReactantMethyl 3-chloro-2-(4-fluorophenyl)quinoxaline-6-carboxylateHCID 77231184—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 70664906HCID 7066490665.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of methyl 3-chloro-2-(4-fluorophenyl)quinoxaline-6-carboxylate (450 mg, 1.42 mmol) in DMSO (5.0 ml) was added 2-(1,2,3,6-tetrahydropyridin-4-yl)pyridine (300 mg, 1.87 mmol) and DIEA (361 mg, 2.79 mmol), and the reaction mixture was stirred overnight at 90° C. The reaction mixture was extracted with ethyl acetate (3×50 ml), and the organic layers combined, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give the residue, which was purified by preparative silica gel plate chromatography (dichloromethane:ethyl acetate:petroleum ether (40:1:12)) to afford methyl 2-(4-fluorophenyl)-3-(4-(pyridin-2-yl)-5,6-dihydropyridin-1(2H)-yl)quinoxaline-6-carboxylate as a yellow solid (410 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-dadf19edba4344e99b77b7b5edf4a823
Source noteuspto-grants-2014_12