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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42806Generated: October 30, 2026

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

https://huagongshe.com/reaction/42806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-nitro-2H-1,2,3-triazoleHCID 278150—
ReactantMethanesulfonic acid 2-(2-methyl-[1,3]dioxolan-2-yl)-pyridin-4-ylmethyl esterHCID 86649484—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(2-Methyl-[1,3]dioxolan-2-yl)-4-(4-nitro-[1,2,3]triazol-2-ylmethyl)-pyridineHCID 67365552—

Reaction Conditions

Temperature50 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of methanesulfonic acid 2-(2-methyl-[1,3]dioxolan-2-yl)-pyridin-4-ylmethyl ester (303 mg, 1.11 mmol) in DMF (2.0 mL) was added to a solution of 4-nitro-2H-[1,2,3]triazole (115 mg, 1.01 mmol) in DMF (2.0 mL) pre-treated for 30 min with DIPEA (0.35 mL, 2.02 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 Na2SO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (5:1 to 2:1 hept-EA) gave the title compound as a pale yellow oil: TLC:rf (1:2 hept-EA)=0.20. LC-MS-conditions 02: tR=0.77 min, [M+H]+=292.24.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536209B2
Source datasetuspto-grants-2013_09
ORD IDord-7ab547e0cb4d4a518b853c5b04aefc86
Source noteuspto-grants-2013_09