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HRID 565935作成日:2026年10月25日

Sodium Thiosulfate → N-(4-(benzylsulfinylmethyl)phenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide

https://huagongshe.com/reaction/565935

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ThiosulfateHCID 24477—
反応物m-Chloroperbenzoic acidHCID 70297—
反応物N-(4-(benzylthiomethyl)phenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamideHCID 18472541—
溶媒DichloromethaneHCID 6344—
生成物N-(4-(benzylsulfinylmethyl)phenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamideHCID 1847244764.6%

反応手順

To a solution of N-(4-(benzylthiomethyl)-phenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide (0.12g) in dichloromethane (25ml) was added 70% m-chloroperbenzoic acid (0.06g) at the temperature ranging from −20 to −10° C., and the mixture was stirred for 10 minutes. To the mixture was added sodium thiosulfate solution, and the mixture was concentrated and extracted with ethyl acetate. The organic layer was washed with sodium hydrogen carbonate solution, water and saturated sodium chloride solution, and dried with anhydrous magnesium sulfate. Under reduced pressure, the solvent was evaporated to give crude crystals, which were recrystallized from ethyl acetate-hexane to give N-(4-(benzylsulfinylmethyl)-phenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide (Compound 109) (0.08g) as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06172061B2
出典データセットuspto-grants-2001_01
ORD IDord-068425301f164ba294c83bbf98b3ca23
出典メモuspto-grants-2001_01