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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1922220Erstellt: 26. Oktober 2026

m-Chloroperbenzoic acid → 2-Pyridinecarboxamide, N-methyl-4-[[2-(methylsulfinyl)-6-benzothiazolyl]oxy]-

https://huagongshe.com/reaction/1922220

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-Chloroperbenzoic acidHCID 70297—
EduktSodium BicarbonateHCID 516892—
EduktN-Methyl-4-((2-(methylthio)benzo[d]thiazol-6-yl)oxy)picolinamideHCID 57725401—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Pyridinecarboxamide, N-methyl-4-[[2-(methylsulfinyl)-6-benzothiazolyl]oxy]-HCID 57725393—

Reaktionsschritte

To the solution of 4-(2-methylsulfanyl-benzothiazol-6-yloxy)-pyridine-2-carboxylic acid methylamide from step 3 (3.88 g, 11.72 mmol, 1.0 eq) in DCM (20 mL) at 0° C., was added MCPBA (77%, 2.88 g, 1. eq). The mixture was stirred at this temperature for one hour. Saturated sodium bicarbonate solution (100 mL) was added. The aqueous layer was extracted with DCM (3×150 mL). The organic layer was dried over sodium sulfate, filtered, and evaporated in vacuo to yield 4-(2-methanesulfinyl-benzothiazol-6-yloxy)-pyridine-2-carboxylic acid methylamide as white powder in quantitative yields. The crude product was used in the next step without purification. M+H=348.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08173689B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-f41a948fbb3e40efb69f55ae4101e4e6
Quellennotizuspto-grants-2012_05