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HRID 971092作成日:2026年10月25日

Phosphoric Acid → (3-[4-(Tert-butoxycarbonyl)piperazin-1-YL]phenyl)boronic acid

https://huagongshe.com/reaction/971092

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphoric AcidHCID 1004—
反応物Triisopropyl borateHCID 21531—
反応物Ammonium ChlorideHCID 25517—
反応物tert-Butyl 4-(3-bromophenyl)piperazine-1-carboxylateHCID 10882380—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒HeptaneHCID 8900—
溶媒Tetrahydrofuran tolueneHCID 22635083—
生成物(3-[4-(Tert-butoxycarbonyl)piperazin-1-YL]phenyl)boronic acidHCID 22392008—

反応条件

温度-78 °C

反応手順

To the 4-tert-Butyloxycarbonyl-1-(3-bromophenyl)piperazine from Step 1 (118.30 g, 346.9 mmol) in tetrahydrofuran/toluene (1/1, 1.5 L) at −78° C. under nitrogen was added n-butyllithium (2.5M, 160 mL, 398.9 mmol) dropwise and the resulting reaction mixture was stirred at −78° C. for 20 minutes. Triisopropyl borate (96.4 mL, 416.3 mmol) was added dropwise and the reaction was warmed to 0° C. and stirred for 2 hours. Aqueous saturated ammonium chloride (400 mL), water (100 mL) and 1 equivalent of H3PO4 (20 mL) were added and the mixture was stirred for 15 minutes and then concentrated to a volume of approximately 200 mL (at which stage the mixture became bluish and a precipitate formed). The mixture was slowly diluted with heptane (800 mL) and the resulting suspension was stirred overnight. The suspension was filtered, the solid was washed with heptane and dried to afford the title boronic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07312334B2
出典データセットuspto-grants-2007_12
ORD IDord-841f4d3d7ddc4b06a2cb958094345a70
出典メモuspto-grants-2007_12