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HRID 748934作成日:2026年10月26日

Nitrogen → (2,6-Dimethoxy-naphthalen-1-yl)-[4-(2-piperidin-1-yl-ethoxy)phenyl]-methanone

https://huagongshe.com/reaction/748934

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物2,6-DimethoxynaphthaleneHCID 79627—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物4-(2-(Piperidin-1-yl)ethoxy)benzoyl chlorideHCID 11119066—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(2,6-Dimethoxy-naphthalen-1-yl)-[4-(2-piperidin-1-yl-ethoxy)phenyl]-methanoneHCID 11654660—

反応条件

温度0 °C

反応手順

Dissolve 2,6-dimethoxynaphthalene (1.0 eq.) in CH2Cl2 (5 volume eq.) at ambient temperature in a dry round bottom flask equipped with stir bar, temperature probe and N2 line. Cool the solution to 0° C. with an ice bath, and add 4-(2-piperidin-1-yl-ethoxy)-benzoyl chloride (1.1 eq.). Add aluminum chloride (2.0 eq.). Once the reaction is determined to be complete, quench the reaction slowly with 1 N NaOH and dilute with additional water and CH2Cl2. Wash the aqueous layer with CH2Cl2 (20 mL). Combine the organic extracts and wash with brine and dry (Na2SO4). Recrystallize the crude product from methanol to give (2,6-dimethoxy-naphthalen-1-yl)-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07399867B2
出典データセットuspto-grants-2008_07
ORD IDord-03b230a1ea134a60b8fda28f8e336702
出典メモuspto-grants-2008_07