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HRID 42225作成日:2026年10月26日

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

https://huagongshe.com/reaction/42225

反応式

関与物質

役割名称HCID仕込み量
反応物HeptaneHCID 8900—
反応物Sodium CarbonateHCID 10340—
反応物4-MethylbenzylamineHCID 66035—
反応物4,5-Bis(bromomethyl)-3,6-dichloropyridazineHCID 57471629—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒TetrahydrofuranHCID 8028—
生成物1,4-dichloro-6-(4-methoxybenzyl)-6,7-dihydro-5H-pyrrolo[3,4-d]pyridazineHCID 5924053641%

反応条件

温度70 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536168B2
出典データセットuspto-grants-2013_09
ORD IDord-5a00fc92a557426b89643e8e79018b9c
出典メモuspto-grants-2013_09