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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 481486생성일: 2026년 10월 26일

Sodium Hydroxide → (2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidine

https://huagongshe.com/reaction/481486

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물5-(1-Cyanocyclopropyl)-2-methoxybenzaldehydeHCID 19066432—
반응물(2S,3S)-2-Phenylpiperidin-3-amine dihydrochlorideHCID 69654807—
용매DichloromethaneHCID 6344—
생성물(2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidineHCID 979904241%

반응 단계

To a stirred suspension of Compound 3 (150 mg, 0.60 mmol) and Compound 2 (145 mg, 0.72 mmol) in dry CH2Cl2 (5 ml) was added NaBH(OAc)3 (358 mg, 1.68 mmol) portionwise at room temperature. The reaction mixture was stirred at room temperature for 6 h. The mixture was basified to pH10-11 with 10% NaOH aq. with ice-cooling. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined solution was washed with brine, dried (MgSO4) and concentrated in vacuo to give crude product. The crude product (300 mg) was purified by column chromatography on silica gel with CH2Cl2 -MeOH (20:1-10:1) to give Compound 4 (89 mg, 41%) as a yellow viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05789423
출처 데이터셋uspto-grants-1998_08
ORD IDord-eb5d9595d0754a179895ec8f0191ad83
출처 메모uspto-grants-1998_08