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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706339Generated: October 29, 2026

Triethylamine → 2,3-Di-p-tolyl-5,6,7,8-tetrahydropyrido[2,3-b]pyrazine

https://huagongshe.com/reaction/706339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,3-Bis(4-methylphenyl)pyrido[2,3-b]pyrazineHCID 4572531—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuran ethanolHCID 21873804—
Product2,3-Di-p-tolyl-5,6,7,8-tetrahydropyrido[2,3-b]pyrazineHCID 66664525—

Reaction Steps

A solution of 2,3-dip-tolylpyrido[2,3-b]pyrazine (step 1) (181 g, 487 mmol) in EtOH/THF (1:2, 2100 ml) was treated with 10% palladium on carbon (30 g, 28.8 mmol) and the reaction mixture was placed under 0.1 bar of hydrogen at RT. After 2 days and 4 days respectively, additional batches of 10% palladium on carbon (10 g, 9.6 mmol, twice) were added along with Et3N (85 ml, 706 mmol, twice). After 7 days in total, the reaction mixture was filtered through Hyflo (filter material) and washed through with THF (2.5 L in portions). The filtrate was concentrated in vacuo to give a green/yellow solid. The solid was triturated with 1:1 TBME/heptane (500 ml) and filtered. The solid was washed with 1:1 TBME/heptane (200 ml) to give a pale yellow solid which was dried overnight to afford the title compound; HPLC (Agilent 1200), Rt 4.73 min, Method B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174985B2
Source datasetuspto-grants-2015_11
ORD IDord-6e98e232e0514a26943d31416cbb9468
Source noteuspto-grants-2015_11