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HRID 3750作成日:2026年10月24日

Allyl bromide → N-allyl-N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide

https://huagongshe.com/ja/reaction/3750

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物Sodium hydrideHCID 24758—
反応物N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxideHCID 20152991—
溶媒DimethylformamideHCID 6228—
生成物N-allyl-N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxideHCID 14097714—

反応手順

To N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide (compound 129, Table A) (1.0 g, 3.0 mmol) in 10 ml of DMF is added NaH (0.30 g, 6.2 mmol) under N2, and the mixture is stirred at RT for 30 minutes. Allyl bromide (0.82 g, 0.59 ml, 6.8 mmol) is added dropwise, and the mixture is stirred at RT for 48 hours. It is then worked up and purified to give the title compound (compound 37, Table A). (DMF is dimethylformamide; RT is room temperature.)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04722749
出典データセットuspto-grants-1988_02
ORD IDord-032d77276ec347c0b8611cfd56e26b51
出典メモuspto-grants-1988_02