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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 383303Erstellt: 25. Oktober 2026

Water → 3-imidazo[1,2-a]pyridine-7-yl-N-methyl-benzamide

https://huagongshe.com/reaction/383303

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CarbonateHCID 10340—
Edukt3-(Methylcarbamoyl)benzeneboronic acidHCID 2773524—
Edukt7-Bromoimidazo(1,2-a)pyridineHCID 15098903—
KatalysatorHCID 178418476HCID 178418476—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt3-imidazo[1,2-a]pyridine-7-yl-N-methyl-benzamideHCID 68484449—

Reaktionsschritte

7-Bromo-imidazo-[1,2-a]-pyridine (1 eq, 0.5 mmol, 100 mg) and (3-methylamino carbonylphenyl)boronic acid (1.1 eq, 0.558 mmol, 99.9 mg) are dissolved in DME (3 ml) and water (0.8 ml) and Na2CO3 (3 eq, 1.52 mmol, 161 mg) is added. PdCl2(PPh3)2 (0.05 eq, 0.025 mmol, 17.8 mg) is then added and the reaction mixture is heated using microwave radiation at 120° C. for 10 min. At the completion of this time the solvent is removed in vacuo and the reaction mixture is purified by flash column chromatography eluting with 9:1 DCM/MeOH to yield 3-imidazo[1,2-a]pyridine-7-yl-N-methyl-benzamide as a brown solid; [M+H]+=252

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367662B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-b91d90e9ac9f49029ba0eea0655cce7b
Quellennotizuspto-grants-2013_02