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HRID 369074作成日:2026年10月25日

Potassium Carbonate → (S)-N-benzylidene-1-[1-(7-bromo-1,4-benzodioxan-2-ylmethyl)-4-piperidyl]methylamine

https://huagongshe.com/reaction/369074

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物N-Benzylidene(piperidin-4-yl)methanamineHCID 11820173—
反応物(R)-7-bromo-1,4-benzodioxan-2-ylmethyl 4-toluenesulphonateHCID 54071671—
触媒Potassium IodideHCID 4875—
溶媒AcetonitrileHCID 6342—
生成物(S)-N-benzylidene-1-[1-(7-bromo-1,4-benzodioxan-2-ylmethyl)-4-piperidyl]methylamineHCID 54401525—

反応手順

A mixture of (R)-7-bromo-1,4-benzodioxan-2-ylmethyl 4-toluenesulphonate (6.5 g, prepared as described in WO97/03071), N-benzylidene-4-piperidylmethylamine (3.0 g), potassium carbonate (4.1 g), and potassium iodide (10 mg) in acetonitrile (200 ml) was heated at reflux, with stirring, under nitrogen for 24 hours. The reaction was cooled, filtered and concentrated under reduced pressure to afford (S)-N-benzylidene-1-[1-(7-bromo-1,4-benzodioxan-2-ylmethyl)-4-piperidyl]methylamine (6.3 g) as an orange-brown viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06136825
出典データセットuspto-grants-2000_10
ORD IDord-92f1ff4b8956456084127daf68f79825
出典メモuspto-grants-2000_10