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HRID 481486作成日:2026年10月27日

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

https://huagongshe.com/reaction/481486

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物5-(1-Cyanocyclopropyl)-2-methoxybenzaldehydeHCID 19066432—
反応物(2S,3S)-2-Phenylpiperidin-3-amine dihydrochlorideHCID 69654807—
溶媒DichloromethaneHCID 6344—
生成物(2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidineHCID 979904241%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05789423
出典データセットuspto-grants-1998_08
ORD IDord-eb5d9595d0754a179895ec8f0191ad83
出典メモuspto-grants-1998_08