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HRID 1675146作成日:2026年10月27日

Triphenylphosphine → 4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperidine

https://huagongshe.com/reaction/1675146

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diisopropyl azodicarboxylateHCID 5363146—
反応物4-Piperidin-4-ylphenolHCID 10511511—
反応物2-(1-methyl-1H-pyrazol-5-yl)ethan-1-olHCID 21832419—
溶媒DichloromethaneHCID 6344—
生成物4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperidineHCID 6734030899.3%

反応条件

温度22 °C

反応手順

DIAD (64.8 μl, 0.33 mmol) was added to 4-(piperidin-4-yl)phenol (CAS 263139-27-1, 53 mg, 0.30 mmol), 2-(1-methyl-1H-pyrazol-5-yl)ethanol (obtained as described in PCT Int. Appl. WO 2007017222, Intermediate 1) (37.7 mg, 0.30 mmol) and triphenylphosphine (86 mg, 0.33 mmol) in DCM (3 mL) at 20° C. under nitrogen. The resulting mixture was stirred at 22° C. for 3 days. The reaction mixture was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M ammonia in methanol and pure fractions were evaporated to dryness to afford 4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperidine (85 mg, 96%) as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08003649B2
出典データセットuspto-grants-2011_08
ORD IDord-64bc66898c944875a16910785de0ea9b
出典メモuspto-grants-2011_08