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HRID 225438作成日:2026年10月26日

2-Bromopropiophenone → 2-[4-(4-Cyclopentyl-piperazine-1-carbonyl)-indol-1-yl]-1-phenyl-propan-1-one

https://huagongshe.com/reaction/225438

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromopropiophenoneHCID 16452—
反応物Sodium t-butoxideHCID 23676156—
反応物HCID 57752820HCID 57752820—
溶媒TetrahydrofuranHCID 8028—
生成物2-[4-(4-Cyclopentyl-piperazine-1-carbonyl)-indol-1-yl]-1-phenyl-propan-1-oneHCID 249912966.1%

反応手順

A mixture of 29.8 mg (0.1 mmol) (4-cyclopentyl-piperazin-1-yl)-(1H-indol-4-yl)-methanone (intermediate 2), 32 mg (0.15 mmol) 2-bromo-1-phenyl-propan-1-one (commercially available) and 28.8 mg (0.3 mmol) sodium-tert-butoxide in 2 mL THF was shaken at room temperature for 16 h. After evaporation to dryness the residue was dissolved in methanol/DMF and subjected to purification by preparative HPLC on reversed phase eluting with a gradient formed from acetonitrile/water/NEt3. The combined product fractions were evaporated to yield 2.6 mg of the title compound. MS (m/e): 430.5 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557108B2
出典データセットuspto-grants-2009_07
ORD IDord-9bff5dfb292542c1991d5bbb57294384
出典メモuspto-grants-2009_07