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

HRID 42779

Reaktionsgleichung

N#N.[CH3:3][C:4]1([C:9]2[CH:14]=[CH:13][N:12]=[C:11]([CH2:15]OS(C)(=O)=O)[CH:10]=2)[O:8][CH2:7][CH2:6][O:5]1.[N+:21]([C:24]1[CH:28]=[N:27][NH:26][N:25]=1)([O-:23])=[O:22].CCN(C(C)C)C(C)C>CN(C=O)C.CC(=O)OCC.O>[CH3:3][C:4]1([C:9]2[CH:14]=[CH:13][N:12]=[C:11]([CH2:15][N:26]3[N:25]=[C:24]([N+:21]([O-:23])=[O:22])[CH:28]=[N:27]3)[CH:10]=2)[O:5][CH2:6][CH2:7][O:8]1

Komponenten

Reaktionsbedingungen

Temperatur: 50 °C

Versuchsvorschrift

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.

Aufarbeitung

additionwere added
extractionThe aq. layer was extracted with EA (10 mL)
dry with materialextracts were dried over NaSO4
filtrationfiltered
customthe solvents were removed under reduced pressure
customPurification of the residue by FC (5:1 to 1:4 hept-EA)

Quellen und Nachweise

ORD-Eintrag: ord-f4592e37c3ff4ed592b3f7d14287cba8
Quelldatensatz: uspto-grants-2013_09
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US08536209B2

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