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HRID 339664作成日:2026年10月26日

Acetic acid;iodosylbenzene → 8-(Tert-butyldimethylsilyloxy)-2-(7-(2-methoxyethoxy)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinoline

https://huagongshe.com/reaction/339664

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic acid;iodosylbenzeneHCID 73357407—
反応物N-[(E)-[8-[tert-butyl(dimethyl)silyl]oxyquinolin-2-yl]methylideneamino]-4-(2-methoxyethoxy)pyridin-2-amineHCID 173055441—
溶媒DichloromethaneHCID 6344—
生成物8-(Tert-butyldimethylsilyloxy)-2-(7-(2-methoxyethoxy)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolineHCID 6723122570%

反応手順

To a solution of (E)-8-(tert-butyldimethylsilyloxy)-2-((2-(4-(2-methoxyethoxy)pyridin-2-yl)hydrazono)methyl)quinoline (0.101 g, 0.223 mmol) in DCM (1.0 mL) was added iodosobenzene diacetate (0.0719 g, 0.223 mmol). After stirring at ambient temperature for 5 hours the reaction mixture was partitioned between DCM and aqueous saturated Na2S2O3. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified via flash column chromatography (40:1 DCM/MeOH) to provide 70 mg (70%) of desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895550B2
出典データセットuspto-grants-2014_11
ORD IDord-53fa496dba3f45c8aa2c6d6a827a1f5f
出典メモuspto-grants-2014_11