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HRID 1690921作成日:2026年10月24日

Sodium Hydroxide → 3-(3-(4-(3-Fluoro-benzyloxy)-benzyl)-isoxazol-5-yl)-pyridin-2-ylamine

https://huagongshe.com/ja/reaction/1690921

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物3-Fluorobenzyl bromideHCID 68007—
反応物4-(5-(2-Amino-pyridin-3-yl)isoxazol-3-ylmethyl)phenolHCID 25114386—
溶媒MethanolHCID 887—
生成物3-(3-(4-(3-Fluoro-benzyloxy)-benzyl)-isoxazol-5-yl)-pyridin-2-ylamineHCID 5762634871.6%

反応手順

To a mixture of 4-(5-(2-amino-pyridin-3-yl)isoxazol-3-ylmethyl)-phenol (4.2 mg, 0.016 mmol) described in Manufacturing Example 5-1-1 and methanol (0.4 mL) was added 1 N aqueous sodium hydroxide solution (16 μL, 0.016 mmol), which was then concentrated under a reduced pressure. To a mixture of the residue and N,N-dimethylformamide (0.5 mL) was added 3-fluorobenzyl bromide (2.3 μL, 0.019 mmol), which was stirred for 1 hour at room temperature. The reaction mixture was purified directly by reverse-phase high performance liquid chromatography (using an acetonitrile-water mobile phase containing 0.1% trifluoroacetic acid) to obtain the title compound (4.3 mg, 55%) as a trifluoroacetic acid salt.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08153662B2
出典データセットuspto-grants-2012_04
ORD IDord-5c4d1bef40b84d8ba61a1c04344494e3
出典メモuspto-grants-2012_04