戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 413023作成日:2026年10月26日

Triethylamine → N-(1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-4-fluorophenylsulfonamide

https://huagongshe.com/reaction/413023

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Fluorobenzenesulfonyl chlorideHCID 9588—
反応物1-[Bis(4-chlorophenyl)methyl]azetidin-3-ylamineHCID 21896598—
溶媒DichloromethaneHCID 6344—
生成物N-(1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-4-fluorophenylsulfonamideHCID 1029854238.7%

反応手順

0.214 g of 4-fluorophenylsulfonyl chloride and 0.28 cm3 of triethylamine are added, at room temperature under an argon atmosphere, to a solution of 0.307 g of 1-[bis(4-chlorophenyl)methyl]azetidin-3-ylamine in 10 cm3 of dichloromethane. After stirring for 16 hours at room temperature, the reaction mixture is washed with 10 cm3 of distilled water, dried over magnesium sulfate, filtered and concentrated to dryness under reduced pressure (2.7 kPa). The residue obtained is purified by flash chromatography on silica gel [eluant: dichloromethane/ethyl acetate (100/0 to 95/5 by volume) gradient]. 0.18 g of N-{1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-4-fluorophenylsulfonamide is obtained in the form of a white foam [1H NMR spectrum (300 MHz, CDCl3, δ in ppm): 2.74 (broad t, J=7.5 Hz: 2H); 2.39 (broad t, J=7.5 Hz: 2H); 3.98 (mt: 1H); 4.20 (s: 1H); 4.79 (d, J=9 Hz: 1H); from 7.10 to 7.35 (mt: 10H); 7.86 (mt: 2H)].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06566356B2
出典データセットuspto-grants-2003_05
ORD IDord-7376a1b4cb4f40fda491fc7e1a49b499
出典メモuspto-grants-2003_05