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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2065038Erstellt: 26. Oktober 2026

Bromide ion → 2-(2-Methyl-[1,3]dioxolan-2-yl)-4-(3-nitro-pyrazol-1-ylmethyl)-thiazole

https://huagongshe.com/reaction/2065038

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromide ionHCID 259—
EduktNitrogenHCID 947—
EduktPotassium CarbonateHCID 11430—
Edukt3-NitropyrazoleHCID 123419—
Edukt4-Chloromethyl-2-(2-methyl-[1,3]dioxolan-2-yl)-thiazoleHCID 66928813—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(2-Methyl-[1,3]dioxolan-2-yl)-4-(3-nitro-pyrazol-1-ylmethyl)-thiazoleHCID 66929202—

Reaktionsschritte

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 4-chloromethyl-2-(2-methyl-[1,3]dioxolan-2-yl)-thiazole (174 mg, 0.79 mmol) in acetone (2.0 mL) was added to a solution of 5-nitro-1H-pyrazole (90 mg, 0.79 mmol) in acetone (2.0 mL). K2CO3 (330 mg, 2.38 mmol) followed by TBA bromide (51 mg, 0.16 mmol) were added and the reaction mixture was stirred at rt overnight. 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 MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (1:1 hept-EA) gave the title compound as a pale yellow oil. TLC: rf (1:1 hept-EA)=0.29. LC-MS-conditions 02: tR=0.89 min, [M+H]+=297.23.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08288419B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-847dc52d889d4f81ac88a42543f6fa0e
Quellennotizuspto-grants-2012_10