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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 239975Erstellt: 24. Oktober 2026

Diisopropylethylamine → Methyl 4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate

https://huagongshe.com/de/reaction/239975

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktPropylphosphonic anhydrideHCID 111923—
EduktBenzoic acid, 4-amino-3,5-dimethyl-, methyl esterHCID 11030398—
Edukt6-Chloro-3-methylpyridine-2-carboxylic acidHCID 46941470—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoateHCID 8670730982,8%

Reaktionsschritte

To a solution of 6-chloro-3-methyl-pyridine-2-carboxylic acid (6.00 g, 0.03508 mol) in CH2Cl2 (50 ml) at 0° C. are added methyl 4-amino-3,5-dimethylbenzoate (5.65 g, 0.03157 mol), and N,N-diisopropylethylamine (15.1 ml, 0.0877 mol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 22.32 g, 0.07016 mol) is added via syringe and stirred at 60° C. After 3 hours, the solvent is removed under reduced pressure and the residue is diluted with water and extracted with ethyl acetate. The organic layers are combined and dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (silica gel) using a gradient of 0-40% ethyl acetate in hexanes to give the title compound as an off-white solid (8.70 g, 74%). Mass spectrum (m/z): 333.2 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642768B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-5fa620b751ca4b1bb62e6844381bd599
Quellennotizuspto-grants-2014_02