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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1675146생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1675146

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물4-Piperidin-4-ylphenolHCID 10511511—
반응물2-(1-methyl-1H-pyrazol-5-yl)ethan-1-olHCID 21832419—
용매DichloromethaneHCID 6344—
생성물4-[4-[2-(1-methyl-1H-pyrazol-5-yl)ethoxy]phenyl]piperidineHCID 6734030899.3%

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온도22 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08003649B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-64bc66898c944875a16910785de0ea9b
출처 메모uspto-grants-2011_08