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HRID 82341생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/82341

반응식

참여 물질

역할이름HCID투입량
반응물EthanolamineHCID 700—
반응물PyridineHCID 1049—
반응물Methanesulfonic anhydrideHCID 81560—
반응물2-(3-(Tert-butoxycarbonyl)phenyl)-3-methylpyridine 1-oxideHCID 58488371—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물Benzoic acid, 3-(6-amino-3-methyl-2-pyridinyl)-, 1,1-dimethylethyl esterHCID 4548051753%

반응 조건

온도10 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846718B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-14d765b789694ef7b1146b515aeb83ba
출처 메모uspto-grants-2014_09