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HRID 42225Erstellt: 24. Oktober 2026

Heptane → 1,4-dichloro-6-(4-methoxybenzyl)-6,7-dihydro-5H-pyrrolo[3,4-d]pyridazine

https://huagongshe.com/de/reaction/42225

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHeptaneHCID 8900—
EduktSodium CarbonateHCID 10340—
Edukt4-MethylbenzylamineHCID 66035—
Edukt4,5-Bis(bromomethyl)-3,6-dichloropyridazineHCID 57471629—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1,4-dichloro-6-(4-methoxybenzyl)-6,7-dihydro-5H-pyrrolo[3,4-d]pyridazineHCID 5924053641%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To a suspension of 4,5-bis(bromomethyl)-3,6-dichloropyridazine (800 mg, 2.39 mmol) in 40 mL anhydrous THF was added with sodium carbonate (507 mg, 4.78 mmol) and tetrabutylammonium iodide (88.3 mg, 0.24 mmol). The reaction mixture was added with 4-methylbenzylamine (0.31 mL, 2.39 mmol) in 20 mL THF dropwisely for 2 h. The reaction mixture was heated at 70° C. for 8 h and concentrated. The crude material was dissolved in DCM and washed with water and brine. The organic solution was dried over Na2SO4 and concentrated to afford a crude oil. The mixture was purified by flash chromatography on silica gel, eluting with 10-80% EtOAc:heptane to afford a off-white solid (300 mg, yield: 41%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536168B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-5a00fc92a557426b89643e8e79018b9c
Quellennotizuspto-grants-2013_09