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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| 반응물 | 1-[Bis(4-chlorophenyl)methyl]azetidin-3-ylamine | HCID 21896598 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-4-fluorophenylsulfonamide | HCID 10298542 | 38.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06566356B2 |
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| 출처 데이터셋 | uspto-grants-2003_05 |
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| ORD ID | ord-7376a1b4cb4f40fda491fc7e1a49b499 |
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| 출처 메모 | uspto-grants-2003_05 |
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