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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1364731Erstellt: 27. Oktober 2026

4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acid → Tert-butyl 4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzylcarbamate

https://huagongshe.com/reaction/1364731

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acidHCID 853605—
Edukt4-Chloro-3-(pyridin-2-yl)anilineHCID 40151925—
ProduktTert-butyl 4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzylcarbamateHCID 66878147—

Reaktionsschritte

75 mg of 4-chloro-3-(pyridin-2-yl)aniline was coupled to 4-((tert-butoxycarbonylamino)methyl)benzoic acid via Procedure G to yield tert-butyl 4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzylcarbamate. Tert-butyl 4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzylcarbamate was subsequently treated with 4N HCl in Dioxane to remove the Boc protecting group and form the HCl salt of 4-(aminomethyl)-N-(4-chloro-3-(pyridin-2-yl)phenyl)benzamide. 50 mg of the crude HCl salt of 4-(aminomethyl)-N-(4-chloro-3-(pyridin-2-yl)phenyl)benzamide was coupled to picolinic acid via Procedure G. The crude product was purified by reverse phase HPLC to yield N-(4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzyl)picolinamide. MS (Q1) 443.3 (M)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07888364B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-f13a954f9a1440a48ddd28327552ea92
Quellennotizuspto-grants-2011_02