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HRID 577780作成日:2026年10月26日

Acetic Acid → (3,5-Bis-trifluoromethyl-benzyl)-[2-(4-cyclohexylmethyl-piperazin-1-yl)-quinolin-3-ylmethyl]-amine

https://huagongshe.com/reaction/577780

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物3,5-Bis(trifluoromethyl)benzylamineHCID 521099—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物2-[4-(Cyclohexylmethyl)piperazin-1-yl]quinoline-3-carbaldehydeHCID 57486817—
溶媒MethanolHCID 887—
生成物(3,5-Bis-trifluoromethyl-benzyl)-[2-(4-cyclohexylmethyl-piperazin-1-yl)-quinolin-3-ylmethyl]-amineHCID 5748681867.4%

反応手順

3,5-Bis(trifluoromethyl)benzylamine (0.305 g, 1.25 mmol) was added to a solution of 2-(4-cyclohexylmethyl-piperazin-1-yl)-quinoline-3-carbaldehyde (0.4 g, 1.23 mmol) in methanol followed by acetic acid (0.15 mL) at ambient temperature under nitrogen atmosphere. After stirring 1 h, sodium cyanoborohydride (0.237 g, 3.77 mmol) was added carefully, and the reaction was stirred at RT for overnight. The reaction mixture was evaporated to dryness, and water (30 mL) and ethyl acetate (30 mL) were added to the residue, and this was then extracted with ethyl acetate (2×30 mL). The combined organic phases were washed with brine, dried over sodium sulfate, filtered, and concentrated under vacuum to afford a pale yellow crude product. Purification by silica gel column chromatography and eluting with 2.5% methanol/dichloromethane afforded the title compound (0.468 g), yield: 67%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040558B2
出典データセットuspto-grants-2015_05
ORD IDord-0a27e504c95b4d2dbe2f0f4bb93f117c
出典メモuspto-grants-2015_05