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HRID 82341Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
EduktPyridineHCID 1049—
EduktMethanesulfonic anhydrideHCID 81560—
Edukt2-(3-(Tert-butoxycarbonyl)phenyl)-3-methylpyridine 1-oxideHCID 58488371—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
ProduktBenzoic acid, 3-(6-amino-3-methyl-2-pyridinyl)-, 1,1-dimethylethyl esterHCID 4548051753%

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846718B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-14d765b789694ef7b1146b515aeb83ba
Quellennotizuspto-grants-2014_09