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HRID 1450433생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1450433

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물[2-Benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl)methanoneHCID 9842862—
반응물HCID 178506676HCID 178506676—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매Cyclohexane diethyletherHCID 21895417—
생성물alpha-[1-[2-(4-Methoxyphenyl)ethyl]-4-piperidinyl]-alpha-phenyl-2-benzothiazolemethanolHCID 18930344—

반응 조건

온도-78 °C

반응 단계

Dissolve [2-benzothiazolyl][1-[2-(4-methoxyphenyl)ethyl]-4piperidinyl]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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05602147
출처 데이터셋uspto-grants-1997_02
ORD IDord-02ba4ab3b5fc4113948ac9c575a83229
출처 메모uspto-grants-1997_02