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HRID 582859作成日:2026年10月26日

Methyl(2-(morpholin-4-yl)ethyl)amine → 6-Methoxy-N-methyl-N-[2-(4-morpholinyl)ethyl]-1,2-benzisoxazol-3-amine

https://huagongshe.com/reaction/582859

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl(2-(morpholin-4-yl)ethyl)amineHCID 14979282—
反応物3-Chloro-6-methoxy-1,2-benzoxazoleHCID 15816924—
生成物6-Methoxy-N-methyl-N-[2-(4-morpholinyl)ethyl]-1,2-benzisoxazol-3-amineHCID 1581692549.4%

反応条件

温度140 °C

反応手順

To a sealed tube was added 3-chloro-6-methoxy-1,2-benzisoxazole (6.0 g) and N-methyl-N-[2-(4-morpholinyl)ethyl]-amine (13.8 g). The reaction was heated to 140° C. over 48 hours and then cooled to room temperature. The residue was partitioned between ethyl acetate (EtOAc) and water, extracted again with EtOAc, and the organic phase was dried over magnesium sulfate (MgSO4) and concentration in vacuo. Flash column chromatography (silica gel) eluting with 1% methanol/dichloromethane (MeOH/DCM) provided the product (4.7 g), m.p. 43-44° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05925766
出典データセットuspto-grants-1999_07
ORD IDord-011f174329cc4dd6bd4aaca930b1b5ca
出典メモuspto-grants-1999_07