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HRID 40641作成日:2026年10月23日

Diisobutylaluminum hydride → Z-(1S,6S)-7-(2,4-Dimethoxy-benzyl)-9-naphthalen-2-yl-7,9-diaza-bicyclo[4.2.2]dec-3-ene

https://huagongshe.com/ja/reaction/40641

反応式

関与物質

役割名称HCID仕込み量
反応物Diisobutylaluminum hydrideHCID 14487—
反応物Z-(1S,6S)-7-(2,4-Dimethoxy-benzyl)-9-naphthalen-2-yl-7,9-diaza-bicyclo[4.2.2]dec-3-ene-8,10-dioneHCID 69230528—
溶媒TetrahydrofuranHCID 8028—
生成物Z-(1S,6S)-7-(2,4-Dimethoxy-benzyl)-9-naphthalen-2-yl-7,9-diaza-bicyclo[4.2.2]dec-3-eneHCID 59686812—

反応条件

温度130 °C

反応手順

Z-(1S,6S)-7-(2,4-Dimethoxy-benzyl)-9-naphthalen-2-yl-7,9-diaza-bicyclo[4.2.2]dec-3-ene-8,10-dione (102 mg, 0.023 mmol), THF (1 mL) and DiBAl-H (6 mL, 6 mmol, [1M]) were placed in a μW tube under argon vent then heated to 130° C. for 900 sec. The reaction was quenched with Rochelle's solution and diethyl ether and the resulting mixture stirred overnight. The organic layer was separated and dried with magnesium sulfate, filtered and the solvent evaporated under reduced pressure to yield a crude oil, which was purified via reverse chromatography (20% CH3CN/water to 100% water) to yield the title compound as a residue.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530475B2
出典データセットuspto-grants-2013_09
ORD IDord-9a469fa7f5324139bbfd8a68ecc1fe1c
出典メモuspto-grants-2013_09