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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1455191Erstellt: 25. Oktober 2026

Sodium Bicarbonate → 2-[[6-Methoxy-3-pyridinyl]methyl]amino-N-[4-bromo-3-(trifluoromethyl)phenyl]benzamide

https://huagongshe.com/reaction/1455191

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
Edukt6-Methoxypyridine-3-carbaldehydeHCID 3364576—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt2-Amino-N-(4-bromo-3-trifluoromethylphenyl)benzamideHCID 11268358—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
Produkt2-[[6-Methoxy-3-pyridinyl]methyl]amino-N-[4-bromo-3-(trifluoromethyl)phenyl]benzamideHCID 9913029—

Reaktionsschritte

Sodium cyanoborohydride (8.80 g of 95%, 133 mmol) is added in portions over 30 minutes to a stirred mixture of acetic acid (3.8 mL), 6-methoxy-3-pyridinecarboxaldehyde (Fluka, Buchs, Switzerland; 7.80 g, 57 mmol) and 2-amino-N-(4-bromo-3-trifluoromethylphenyl)-benzamide (step 1.2; 13.65 g, 38 mmol) in methanol (380 mL) at 25° C. The mixture is stirred for 16 hours. The solvent is evaporated under reduced pressure to give a residue which is treated with a saturated aqueous solution of sodium hydrogen carbonate (500 mL) and extracted with dichloromethane (3×150 mL). The combined extracts are dried (Na2SO4), filtered and the solvent is evaporated under reduced pressure to yield the crude product that is purified by column chromatography on silica gel, eluent 5% ethyl acetate in dichloromethane and recrystallised from diethylether—hexane to give the title compound as a beige crystalline solid, m.p. 101-103° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07482369B2
Quelldatensatzuspto-grants-2009_01
ORD IDord-a6b14e618b9246f19c26541aec44224f
Quellennotizuspto-grants-2009_01