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HRID 2064969Erstellt: 25. Oktober 2026

Nitrogen → 2-(2-Methyl-[1,3]dioxolan-2-yl)-6-(3-nitro-pyrazol-1-ylmethyl)-pyridine

https://huagongshe.com/reaction/2064969

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktPotassium CarbonateHCID 11430—
EduktIodide IonHCID 30165—
Edukt3-NitropyrazoleHCID 123419—
EduktMethanesulfonic acid 6-(2-methyl-[1,3]dioxolan-2-yl)-pyridin-2-ylmethyl esterHCID 86649482—
LösungsmittelAcetoneHCID 180—
Produkt2-(2-Methyl-[1,3]dioxolan-2-yl)-6-(3-nitro-pyrazol-1-ylmethyl)-pyridineHCID 66928714—

Reaktionsschritte

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of methanesulfonic acid 6-(2-methyl-[1,3]dioxolan-2-yl)-pyridin-2-ylmethyl ester (273 mg, 1.00 mmol) in acetone (4.0 mL) was added, under inert atmosphere (N2) to a solution of 5-nitro-1H-pyrazole (115 mg, 1.00 mmol) in acetone (4.0 mL). K2CO3 (698 mg, 5.00 mmol) and TBA iodide (64 mg, 0.20 mmol) were added and the reaction mixture was stirred at rt for 5 h. The solvent was removed under reduced pressure. Water (10 mL) and EA (10 mL) were added. The aq. layer was extracted with EA (10 mL) and the combined org. extracts were dried over Na2SO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (30:10 to 50:50 hept-EA) gave the title compound as a light brown solid. TLC: rf (50:50 hept-EA)=0.16. LC-MS-conditions 02: tR=0.87 min; [M+H]+=291.35.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08288419B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-50b2537267d3483dae73d0f0115722cf
Quellennotizuspto-grants-2012_10