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HRID 82341作成日:2026年10月26日

Ethanolamine → Benzoic acid, 3-(6-amino-3-methyl-2-pyridinyl)-, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/82341

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolamineHCID 700—
反応物PyridineHCID 1049—
反応物Methanesulfonic anhydrideHCID 81560—
反応物2-(3-(Tert-butoxycarbonyl)phenyl)-3-methylpyridine 1-oxideHCID 58488371—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物Benzoic acid, 3-(6-amino-3-methyl-2-pyridinyl)-, 1,1-dimethylethyl esterHCID 4548051753%

反応条件

温度10 °C

反応手順

A solution of 2-(3-(tert-butoxycarbonyl)phenyl)-3-methylpyridine-1-oxide (1 eq) and pyridine (4 eq) in MeCN (8 vol) is heated to 70° C. A solution of methanesulfonic anhydride (1.5 eq) in MeCN (2 vol) is added over 50 min via addition funnel maintaining the temperature at less than 75° C. The mixture is stirred for an additional 0.5 hours after complete addition. The mixture is then allowed to cool to ambient. Ethanolamine (10 eq) is added via addition funnel. After stirring for 2 hours, water (6 vol) is added and the mixture is cooled to 10° C. After stirring for NLT 3 hours, the solid is collected by filtration and washed with water (3 vol), 2:1 MeCN/water (3 vol), and MeCN (2×1.5 vol). The solid is dried to constant weight (<1% difference) in a vacuum oven at 50° C. with a slight N2 bleed to afford tert-butyl-3-(6-amino-3-methylpyridin-2-yl)benzoate as a red-yellow solid (53% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846718B2
出典データセットuspto-grants-2014_09
ORD IDord-14d765b789694ef7b1146b515aeb83ba
出典メモuspto-grants-2014_09