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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 877643생성일: 2026년 10월 23일

1-(5-Chloro-2-nitrophenyl)ethanone → N-[(E)-1-(5-chloro-2-nitrophenyl)ethylideneamino]-3-morpholin-4-ylsulfonylbenzamide

https://huagongshe.com/ko/reaction/877643

반응식

참여 물질

역할이름HCID투입량
반응물1-(5-Chloro-2-nitrophenyl)ethanoneHCID 255582—
반응물3-(Morpholine-4-sulfonyl)benzohydrazideHCID 877246—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물N-[(E)-1-(5-chloro-2-nitrophenyl)ethylideneamino]-3-morpholin-4-ylsulfonylbenzamideHCID 8658106320.09%

반응 조건

온도120 °C

반응 단계

1-(5-chloro-2-nitrophenyl)ethanone (30 mg, 0.150 mmol) and 3-(morpholinosulfonyl)benzohydrazide (42.9 mg, 0.150 mmol) was dissolved in Methanol (Volume: 4 ml) in the presence of acetic acid as a catalyst and then the reaction mixture was heated via microwave irradiation to 120° C. for 30 min. Reaction was monitored by TLC. After completion of the reaction, following cooling, the solvent was removed by vacuum and the resulting crude material was purified by flash column chromatography (2% CH3OH/CH2Cl2), afforded the product (E)-N′-(1-(5-chloro-2-nitrophenyl)ethylidene)-3-(morpholinosulfonyl)benzohydrazide (15 mg, 0.030 mmol, 20.09% yield) as a solid. 1H NMR (CDCl3, 400 MHz): δ 8.20 (m, 1H), 8.07 (m, 1H), 7.88 (m, 1H), 7.66 (m, 1H), 7.51 (m, 2H), 7.39 (m, 1H), 3.69 (m, 4H), 2.99 (m, 4H), 2.29 (s, 3H). Mass [M+H]+:468.0

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987335B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-f869f224d2614839b7c33efbcc64afde
출처 메모uspto-grants-2015_03