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HRID 42779Erstellt: 24. Oktober 2026

Nitrogen → 4-(2-Methyl-[1,3]dioxolan-2-yl)-2-(4-nitro-[1,2,3]triazol-2-ylmethyl)-pyridine

https://huagongshe.com/de/reaction/42779

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktDiisopropylethylamineHCID 81531—
Edukt4-nitro-2H-1,2,3-triazoleHCID 278150—
EduktMethanesulfonic acid 4-(2-methyl-[1,3]dioxolan-2-yl)-pyridin-2-ylmethyl esterHCID 86649481—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-(2-Methyl-[1,3]dioxolan-2-yl)-2-(4-nitro-[1,2,3]triazol-2-ylmethyl)-pyridineHCID 67363839—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of methanesulfonic acid 4-(2-methyl-[1,3]dioxolan-2-yl)-pyridin-2-ylmethyl ester (315 mg, 1.15 mmol) in DMF (2.0 mL) was added to a solution of 4-nitro-2H-[1,2,3]triazole (120 mg, 1.05 mmol) in DMF (2.0 mL) pre-treated for 30 min with DIPEA (0.36 mL, 2.10 mmol) and the reaction mixture was stirred for 48 h at 50° C. Water (10 mL), followed by EA (10 mL) were added. The aq. layer was extracted with EA (10 mL) and the combined org. extracts were dried over NaSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (5:1 to 1:4 hept-EA) gave the title compound as a pale yellow solid: TLC:rf (1:2 hept-EA)=0.24. LC-MS-conditions 02: tR=0.89 min, [M+H]+=292.27.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536209B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-f4592e37c3ff4ed592b3f7d14287cba8
Quellennotizuspto-grants-2013_09