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HRID 22739作成日:2026年10月24日

Diisopropylamine → 3-Methoxy-6-(3-hydroxy-benzofuran-2-sulfonyl)-pyridazine

https://huagongshe.com/ja/reaction/22739

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物CoumaranoneHCID 23556—
反応物3-Fluorosulfonyl-6-methoxypyridazineHCID 11030636—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物3-Methoxy-6-(3-hydroxy-benzofuran-2-sulfonyl)-pyridazineHCID 1207176517%

反応条件

温度-78 °C

反応手順

n-Butyl lithium (12 mmol, 4.7 mL) was added dropwise to a solution of diisopropyl amine (12 mmol, 1.7 mL) in THF (5 mL) at −78° C. After 10 minutes, a solution of 3-coumaranone (10 mmol, 1.92 g) in THF (10 mL) was added. The temperature was maintained at −78° C. and stirred for 10 minutes. To this was added a solution of 3-fluorosulfonyl-6-methoxy-pyridazine. The reaction mixture was brought to room temperature over one hour and quenched with ammonium chloride (1 g) and extracted with EtOAc (2×25 mL). The EtOAc extract was washed with H2O, the organic layer was collected, dried, filtered and the filtrate was evaporated to a residue. This residue was purified by silica gel chromatography (eluent:hexanes:EtOAc::9:1) to yield 3-methoxy-6-(3-hydroxy-benzofuran-2-sulfonyl)-pyridazine (17%, 622 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849629B2
出典データセットuspto-grants-2005_02
ORD IDord-d33ee970cf0e419886cf788bf37573d3
出典メモuspto-grants-2005_02