戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2064183作成日:2026年10月26日

Triphenylphosphine → N-(5-Ethenyl-4-fluoro-2-nitrophenyl)-1-(tetrahydro-2H-pyran-4-yl)-4-piperidinamine

https://huagongshe.com/reaction/2064183

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物N-(5-Bromo-4-fluoro-2-nitrophenyl)-1-(tetrahydro-2H-pyran-4-yl)-4-piperidinamineHCID 59850147—
触媒(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
溶媒TolueneHCID 1140—
生成物N-(5-Ethenyl-4-fluoro-2-nitrophenyl)-1-(tetrahydro-2H-pyran-4-yl)-4-piperidinamineHCID 59850136314.8%

反応条件

温度130 °C

反応手順

A solution of N-(5-bromo-4-fluoro-2-nitrophenyl)-1-(tetrahydro-2H-pyran-4-yl)-4-piperidinamine (D78, 800 mg, ˜75% purity) and n-tributylvinyltin (0.697 ml, 2.3 mmol) in toluene (30 ml) was treated, under a positive flow of argon, with triphenylphosphine (129.8 mg, 0.5 mmol) and bis(dibenzylideneacetone)palladium(0) (170.1 mg, 0.297 mmol), then stirred and heated under argon atmosphere at 130° C. for 1.5 h. The mixture was filtered through a celite pad. The organic layer was washed with NH4OH (10% aq) and water, then dried over MgSO4 and concentrated. The mixture was purified on silica column (100 g of silica, methanol/dichloromethane, 5% to 20%, 15CV) to afford 550 mg of title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08288412B2
出典データセットuspto-grants-2012_10
ORD IDord-cd3d7f9b8fec466bb48faa051fdb128f
出典メモuspto-grants-2012_10