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HRID 1294714作成日:2026年10月26日

Pyridine → 2,4-Dinitrobenzenesulfonamide

https://huagongshe.com/reaction/1294714

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Trifluoroacetic acidHCID 6422—
反応物Sulfuryl chlorideHCID 24648—
反応物Benzenesulfonyl chloride, 2,4-dinitro-HCID 74255—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物2,4-DinitrobenzenesulfonamideHCID 10911854—

反応手順

A solution of Part A compound (1.01 g, 2.37 mmol) and TFA (8 mL) in CH2Cl2 (30 mL) was stirred at RT for 4.5 h. The solution was concentrated in vacuo, and the residue was dissolved in CH2Cl2 and filtered through a pad of solid K2CO3. The filtrate was concentrated in vacuo to give the corresponding crude amine. To a solution of the crude amine in THF (11.9 mL) were added pyridine (0.383 mL, 4.74 mmol) and 2,4-dinitrobenzenesulfonyl chloride (0.85 g, 3.19 mmol) and the solution was stirred at RT for 15 h. Since some starting material still remained at this point, more sulfonyl chloride (0.32 g, 1.2 mmol) was then added. After a further 4 h, HPLC analysis indicated that all starting material had been consumed. The reaction mixture was diluted with Et2O, washed with 1N aq HCl, saturated aq NaHCO3 and brine, dried (MgSO4), filtered and concentrated in vacuo to provide the crude 2,4-dinitrobenzenesulfonamide

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07241780B2
出典データセットuspto-grants-2007_07
ORD IDord-9a6f3c68a27c48d99b239b56849d49a4
出典メモuspto-grants-2007_07