Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605590Generated: November 3, 2026

Triethylamine → HCID 59152162, compound

https://huagongshe.com/reaction/605590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
ReactantN-(1-(tert-Butyl)-1H-pyrazol-5-yl)-6-chloropyrazin-2-amineHCID 59152183—
Solvent1-PropanolHCID 1031—
ProductHCID 59152162HCID 59152162—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 65.04 g of N-(1-tert-butyl-1H-pyrazol-5-yl)-6-chloropyrazin-2-amine, 41.6 g of potassium vinyltrifluoroborate, 4.22 g of (1,1′-bis (diphenylphosphino)ferrocene)dichloropalladium(II) dichloromethane complex, 72 ml of triethylamine and 685 ml of 1-propanol was stirred at 110° C. overnight, followed by cooling down to room temperature and concentrated in vacuo. The obtained residue was diluted with ethyl acetate, and an insoluble matter was filtered off using Celite. The resulting ethyl acetate solution was washed with water, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo. The obtained residue was suspended in 100 ml of ethyl acetate, and 400 ml of diisopropylether was added to the mixture. The obtained precipitate was collected to give the title compound as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915263B2
Source datasetuspto-grants-2011_03
ORD IDord-796fb5c675cc485293f5af6b0cf0d8dd
Source noteuspto-grants-2011_03