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HRID 266093作成日:2026年10月26日

Methane → alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-phenyl-2-benzothiazolemethanol

https://huagongshe.com/reaction/266093

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物[2-Benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl)methanoneHCID 9842862—
反応物HCID 178506676HCID 178506676—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
溶媒Cyclohexane diethyletherHCID 21895417—
生成物alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-phenyl-2-benzothiazolemethanolHCID 18930344—

反応条件

温度-78 °C

反応手順

Dissolve [2-benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]methanone (2.0 g, 5.26 mmol) in anhydrous tetrahydrofuran (50 mL), place under an argon atmosphere and cool to -78° C. Add, by dropwise addition, phenyllithium (3.16 mL of a 2.0M solution in cyclohexane/ethyl ether, 6.31 mmol). Stir at -78° C. for 30 minutes, quench with saturated ammonium chloride (100 mL), separate the organic phase and extract the aqueous phase with ethyl acetate. Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo. Purify by chromatography (75% ethyl acetate/hexane) to give a yellow oil. Dissolve the oil in methylene chloride and treat with activated charcoal.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05650416
出典データセットuspto-grants-1997_07
ORD IDord-89916258f28a42408349c04189ac3716
出典メモuspto-grants-1997_07