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HRID 2370513作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/2370513

反応式

関与物質

役割名称HCID仕込み量
反応物m-Chloroperbenzoic acidHCID 70297—
反応物Sodium BicarbonateHCID 516892—
反応物N-Methyl-4-((2-(methylthio)benzo[d]thiazol-6-yl)oxy)picolinamideHCID 57725401—
溶媒DichloromethaneHCID 6344—
生成物2-Pyridinecarboxamide, N-methyl-4-[[2-(methylsulfinyl)-6-benzothiazolyl]oxy]-HCID 57725393—

反応手順

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, 1.1 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08710048B2
出典データセットuspto-grants-2014_04
ORD IDord-bc512e3c69a84843a9eef4cf67443585
出典メモuspto-grants-2014_04