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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 922851Erstellt: 26. Oktober 2026

Acetic Acid → N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-((dimethylamino)methyl)benzamide

https://huagongshe.com/reaction/922851

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktFormaldehydeHCID 712—
EduktDimethylformamideHCID 6228—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt4-(aminomethyl)-N-(4-chloro-3-(pyridin-2-yl)phenyl)benzamideHCID 66877992—
ProduktN-(4-chloro-3-(pyridin-2-yl)phenyl)-4-((dimethylamino)methyl)benzamideHCID 58614907—

Reaktionsschritte

Procedure G was used to couple BOC-4-(aminomethyl)benzoic acid (48 mg) with 4-chloro-3-(pyridin-2-yl)aniline (35 mg). The crude reaction mixture was treated with TFA (1 mL) containing trace amounts of water for 1 h. The reaction mixture was concentrated to yield 4-(aminomethyl)-N-(4-chloro-3-(pyridin-2-yl)phenyl)benzamide. 4-(aminomethyl)-N-(4-chloro-3-(pyridin-2-yl)phenyl)benzamide (80 mg) was dissolved in DMF (5 mL) and treated with AcOH (10 L), paraformaldehyde (48 mg), and sodium triacetoxyborohydride (125 mg) for 16 h. The reaction mixture was concentrated, and the crude residue was dissolved in ethyl acetate and washed with 1 N sodium hydroxide, dried (MgSO4) and concentrated. The crude product was purified by reverse phase HPLC to yield N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-((dimethylamino)methyl)benzamide. MS (Q1) 365.0 (M)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09278961B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-a98e85eabba64752bf14d90ebc9bb51e
Quellennotizuspto-grants-2016_03