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HRID 2149作成日:2026年10月24日

Methyl bromoacetate → [4-(3-Benzo[d]isoxazolylimino)-1-(4H)-pyridinyl]-acetic acid methyl ester hydrobromide

https://huagongshe.com/ja/reaction/2149

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl bromoacetateHCID 60984—
反応物1,2-Benzisoxazol-3-amine, N-4-pyridinyl-HCID 9837219—
溶媒AcetonitrileHCID 6342—
生成物[4-(3-Benzo[d]isoxazolylimino)-1-(4H)-pyridinyl]-acetic acid methyl ester hydrobromideHCID 7028062570%

反応手順

A mixture of 3-(4-pyridinylamino)-1,2-benzisoxazole (0.9 g, 4.3 mmol) and methyl bromoacetate (0.44 mL, 1.1 eq) in acetonitrile (25 mL) was heated at reflux for one hour. The mixture was then allowed to cool to room temperature and the precipitated product was collected by filtration. The white solid was washed with diethyl ether and dried under vacuum to provide the title compound (1.1 g, 70%), mp 235-236° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728717
出典データセットuspto-grants-1998_03
ORD IDord-dc610c599a6a47cbbab5dcc6ac8c553a
出典メモuspto-grants-1998_03