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HRID 8692作成日:2026年10月24日

Amantadine → Adamantan-1-yl-[3-(3-thieno[2,3-d]isoxazol-3-yl-phenoxy)-propyl]-amine

https://huagongshe.com/ja/reaction/8692

反応式

関与物質

役割名称HCID仕込み量
反応物AmantadineHCID 2130—
反応物Potassium CarbonateHCID 11430—
反応物3-[3-(3-Bromo-propoxy)phenyl]-thieno[2,3-d]isoxazoleHCID 21983559—
溶媒AcetonitrileHCID 6342—
生成物Adamantan-1-yl-[3-(3-thieno[2,3-d]isoxazol-3-yl-phenoxy)-propyl]-amineHCID 2198359944%

反応条件

温度75 °C

反応手順

Mix 3-[3-(3-bromo-propoxy)-phenyl]-thieno[2,3-d]isoxazole (0.250 g, 0.739 mmol), potassium carbonate (0.205 g, 1.48 mmol), 1-adamantanamine (0.560 g, 3.70 mmol) and acetonitrile (4.0 mL) and heat at 75° C., overnight. Cool the reaction mixture and filter through a Waters Sep-Pak (1 g) silica gel cartridge (ethyl acetate). Combine the appropriate fractions and concentrate to give a residue. Purify the residue by column (10 g silica) chromatography using a step gradient from 40% ethyl acetate in dichloromethane to 100% ethyl acetate to 20% methanol in ethyl acetate to give the title compound (132 mg, 44% yield). Purity by LC/MS (APCI)=98%, [M+H]+=409.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091199B1
出典データセットuspto-grants-2006_08
ORD IDord-7b4bedc2459741bd84e5d05b7da325ca
出典メモuspto-grants-2006_08