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HRID 252208Erstellt: 26. Oktober 2026

Triethylamine → Methyl 2-{[(5-methylpyridin-3-yl)amino]sulfonyl}benzoate

https://huagongshe.com/reaction/252208

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktBenzoic acid, 2-(chlorosulfonyl)-, methyl esterHCID 117830—
Edukt3-Amino-5-methylpyridineHCID 2762894—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelSodium BicarbonateHCID 516892—
ProduktMethyl 2-{[(5-methylpyridin-3-yl)amino]sulfonyl}benzoateHCID 5892407334%

Reaktionsschritte

To a solution of 5-methylpyridin-3-amine (0.5 g, 4.62 mmol) in CH2Cl2 (50 ml) were added triethylamine (0.64 mL, 4.62 mmol) and methyl 2-(chlorosulfonyl)benzoate (1.08 g, 4.62 mmol). The resulting mixture was stirred at room temperature for 1 hour. The mixture was then diluted with saturated aqueous NaHCO3 and extracted with CH2Cl2. The organic layer was dried over Na2SO4, filtered and concentrated. The crude residue was purified by flash chromatography (0-8% MeOH/CH2Cl2) to give the title compound (0.476 g, 34%). 1H NMR (400 MHz, DMSO-D6) δ ppm 10.25-10.62 (m, 1H) 8.6 (s, 2H) 7.81-7.93 (m, 1H) 7.64-7.76 (m, 2H) 7.54-7.64 (m, 1H) 7.28 (s, 1H) 3.80 (s, 3H) 2.18 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07868026B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-6f001939915e4bf99a8728db4c5e78d8
Quellennotizuspto-grants-2011_01