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HRID 567948作成日:2026年10月26日

Monoperoxyphthalic Acid Magnesium Salt → 4-{2-[3,4-Bis(difluoromethoxy)phenyl]-2-{6-[4-(trifluoromethoxy)phenoxy]-3-pyridyl}ethyl}pyridine-N-oxide

https://huagongshe.com/reaction/567948

反応式

関与物質

役割名称HCID仕込み量
反応物Monoperoxyphthalic Acid Magnesium SaltHCID 10130449—
反応物4-{2-[3,4-Bis(difluoromethoxy)phenyl]-2-{6-[4-(trifluoromethoxy)phenoxy]-3-pyridyl}ethyl}pyridineHCID 21262788—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物4-{2-[3,4-Bis(difluoromethoxy)phenyl]-2-{6-[4-(trifluoromethoxy)phenoxy]-3-pyridyl}ethyl}pyridine-N-oxideHCID 21262804162%

反応手順

To a solution of 4-{2-[3,4-bis(difluoromethoxy)phenyl]-2-{6-[4-(trifluoromethoxy)phenoxy]-3-pyridyl}ethyl}pyridine (340 mg, 0.598 mmol) from Step 5 above in a mixture of 6 mL of CH2Cl2 and 0.6 mL of MeOH, was added MMPP (222 mg, 0.359 mmol) in one portion. The mixture was stirred 24 h at room temperature and the reaction was completed with an other 50 mg of MMPP. The reaction was quenched with a saturated aqueous NaHCO3 solution and diluted with CH2Cl2. The organic layer was washed with brine, dried over MgSO4 and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (5% MeOH/CH2Cl2) to afford the title compound as an amorphous solid (340 mg, 97%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06180650B2
出典データセットuspto-grants-2001_01
ORD IDord-ebb6f3d8ed0940de80ad1768c155f568
出典メモuspto-grants-2001_01