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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413023생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/413023

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Fluorobenzenesulfonyl chlorideHCID 9588—
반응물1-[Bis(4-chlorophenyl)methyl]azetidin-3-ylamineHCID 21896598—
용매DichloromethaneHCID 6344—
생성물N-(1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-4-fluorophenylsulfonamideHCID 1029854238.7%

반응 단계

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)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06566356B2
출처 데이터셋uspto-grants-2003_05
ORD IDord-7376a1b4cb4f40fda491fc7e1a49b499
출처 메모uspto-grants-2003_05