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HRID 561708作成日:2026年10月25日

(4-Chlorophenyl)(4-fluorophenyl)methanol → 3-[(4-Chlorophenyl)(4-fluorophenyl)methyl]-5-fluoro-7-[(methylsulfanyl)methyl]-1H-indole

https://huagongshe.com/reaction/561708

反応式

関与物質

役割名称HCID仕込み量
反応物(4-Chlorophenyl)(4-fluorophenyl)methanolHCID 12634874—
反応物3-[Bis(4-fluorophenyl)methyl]-7-[(methylsulfanyl)methyl]-1H-indoleHCID 58392127—
反応物5-Fluoro-7-[(methylsulfanyl)methyl]-1H-indoleHCID 58392227—
生成物3-[(4-Chlorophenyl)(4-fluorophenyl)methyl]-5-fluoro-7-[(methylsulfanyl)methyl]-1H-indoleHCID 58392172—

反応条件

温度80 °C

反応手順

The title compound was prepared starting from 500 mg (2.56 mmol) of the compound from Example 11A and 667 mg (2.56 mmol) of the compound from Example 81A in analogy to the synthesis of the compound from Example 278. A difference was that stirring at 80° C. was for only 4 h. 535 mg (50% of theory) of the target compound were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063234B2
出典データセットuspto-grants-2011_11
ORD IDord-96b97a45989947df83e8d72184099e7e
出典メモuspto-grants-2011_11