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HRID 900774作成日:2026年10月26日

Hexane → 1-cycloheptyl-3-[(3R)-3-methoxy-1-azabicyclo[2.2.2]oct-3-yl]-1-phenyl-2-propyn-1-ol

https://huagongshe.com/reaction/900774

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Cycloheptyl(phenyl)methanoneHCID 297753—
反応物(3R)-3-ethynyl-1-azabicyclo[2.2.2]oct-3-yl methyl etherHCID 9812856—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-cycloheptyl-3-[(3R)-3-methoxy-1-azabicyclo[2.2.2]oct-3-yl]-1-phenyl-2-propyn-1-olHCID 69292392—

反応条件

温度-5 °C

反応手順

A 1.6 N solution of BuLi in hexane (41.7 ml, 66.7 mmol) was added dropwise to a solution of (3R)-3-ethynyl-1-azabicyclo[2.2.2]oct-3-yl methyl ether 53 (11 g, 66.7 mmol) in THF (100 ml) cooled at −5° C. After stirring for 10 minutes, the medium was cooled at −15° C., and a solution of cycloheptyl(phenyl)methanone 44 (14.2 g, 70.2 mmol) in THF (50 ml) was slowly added. The cooling bath was removed and the reaction was allowed to gradually warm to room temperature during 2 hours. The reaction was quenched by the addition of saturated aqueous NH4Cl solution. The reaction mixture was washed with brine, dried over Na2SO4 and evaporated. The yellowish oil was purified by chromatography over silica gel (CH2Cl2/EtOH/NH4OH 94/6/1). 1-cycloheptyl-3-[(3R)-3-methoxy-1-azabicyclo[2.2.2]oct-3-yl]-1-phenyl-2-propyn-1-ol 116 was obtained as a white solid (20.35 g, 83%, mixture of diastereomers).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07361668B2
出典データセットuspto-grants-2008_04
ORD IDord-0b5f7c8ca8064a15b6e47d696e40695f
出典メモuspto-grants-2008_04