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HRID 83022作成日:2026年10月24日

Triethylamine → 5-Bromo-3-((2-(4-methylpiperazin-1-yl)ethylamino)methyl)pyridin-2-amine

https://huagongshe.com/ja/reaction/83022

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Methylpiperazine-1-ethylamineHCID 70284—
反応物Sodium borohydrideHCID 4311764—
反応物2-Amino-5-bromonicotinaldehyde hydrobromideHCID 86606146—
溶媒MethanolHCID 887—
生成物5-Bromo-3-((2-(4-methylpiperazin-1-yl)ethylamino)methyl)pyridin-2-amineHCID 67154522—

反応条件

温度0 °C

反応手順

Triethylamine (1.0 mL, 7.09 mmol) was added to a solution of 2-amino-5-bromonicotinaldehyde hydrobromide (1.0 g, 3.54 mmol) in methanol (24 mL) at room temperature. The reaction mixture was stirred for 10 minutes prior to the addition of 2-(4-methylpiperazin-1-yl)ethanamine (558 mg, 3.90 mmol). The reaction mixture was then stirred overnight and cooled to 0° C. Sodium borohydride (201 mg, 5.32 mmol) was added portionwise at 0° C. and the reaction mixture was allowed to reach room temperature and stirred for 4 hours. After concentration to dryness, the residue was purified by chromatography on silica gel using dichloromethane/methanol/ammoniac (10:0:0.1 to 9:1:0.1) as eluent. The title product was obtained as a yellow solid (560 mg, 48%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846711B2
出典データセットuspto-grants-2014_09
ORD IDord-39900b3f3ff04ae5b23668af34e3bc84
出典メモuspto-grants-2014_09