Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33843Generated: October 27, 2026

Triphenylphosphine → 2-[4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinoxaline

https://huagongshe.com/reaction/33843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
ReactantQuinoxalin-2-ylmethanolHCID 905614—
Reactant4-[1-methyl-4-(4-pyridinyl)-1H-pyrazol-3-yl]PhenolHCID 135915213—
Solvent1,4-DioxaneHCID 31275—
Product2-[4-(1-Methyl-4-pyridin-4-yl-1H-pyrazol-3-yl)-phenoxymethyl]-quinoxalineHCID 1154564169%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-(1-Methyl4-pyridin-4-yl-1H-pyrazol-3-yl)-phenol (50 mg) in dioxane (2 ml) was added triphenylphosphine (84 mg), quinoxaline-2-yl-methanol (48 mg) and di-t-butyl-aza-dicarboxylate (73 mg) and the reaction mixture was heated at 60° C. for 18 h. The reaction mixture was poured into 1N NaOH, extracted 3× methylene chloride, dried magnesium sulfate, filtered and concentration Purification via MPLC biotage chromatography provided the title compound (54 mg, 67%). 1H NMR (400 MHz, CDCl3) δ 9.09 (s, 1H), 8.45 (d, J=6.2 Hz, 2H), 8.10 (m, 2 H), 7.77 (m, 2H), 7.55 (s, 1H), 7.37 (d, J=9.1 Hz, 2H), 7.10 (d, J=6.9 Hz, 2 H), 7.01 (d, J=8.7, 2H), 5.41 (s, 2 H), 3.94 (s, 3H); MS: (M+H m/z=394.4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429665B2
Source datasetuspto-grants-2008_09
ORD IDord-382eac61ff9c4471afec32cc675cbb78
Source noteuspto-grants-2008_09