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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296628Generated: October 31, 2026

Phenol → HCID 18186854, compound

https://huagongshe.com/reaction/1296628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-6-(1-piperazinyl)pyrazineHCID 107992—
SolventChloroformHCID 6212—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 18186854HCID 18186854—

Reaction Conditions

Temperature165 °C

Reaction Steps

A mixture of the product obtained in example 13, step 2 (1.97 g, 9.92 mmol), phenol (2.43 g, 25.8 mmol), CuO (1.0 g, 12.6 mmol), and K2CO3 (1.43 g, 10.3 mmol) in dioxane (2 mL) was stirred for 4.5 h at 165° C. in a sealed pyrex tube. The reaction mixture was diluted with CHCl3 and filtered through a pad of Celite. The pad was washed with several portions of CHCl3/MeOH (95:5). Solvent removal in vacuo furnished a dark brown oil which was purified by column chromatography on silica gel (14×5 cm) using CHCl3/MeOH (95:5, followed by 90:10) as eluent. The brown oil (1.66 g) was subjected to repeated column chromatography, first on silica gel (18×4 cm) using CHCl3/MeOH (9:1) as eluent and finally on alumina (4×5 cm) using ether/MeOH (95:5) as eluent. This furnished 1.37 g (54%) of the title compound as a light beige oil. HRMS m/z calcd for C14H16N4O (M)30 256.1324, found 256.1321. Anal. (C14H16N4O) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247633B2
Source datasetuspto-grants-2007_07
ORD IDord-db2ada8d78e14f8799547893688e05ae
Source noteuspto-grants-2007_07