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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 365372생성일: 2026년 10월 25일

1-(1-Naphthyl)piperazine → 6-(2-(4-(1-Naphthyl)-piperazinyl)ethyl)benzothiazolone

https://huagongshe.com/reaction/365372

반응식

참여 물질

역할이름HCID투입량
반응물1-(1-Naphthyl)piperazineHCID 1342—
반응물Sodium CarbonateHCID 10340—
반응물6-(2-Bromoethyl)benzothiazoloneHCID 69227973—
용매Methyl Isobutyl KetoneHCID 7909—
생성물6-(2-(4-(1-Naphthyl)-piperazinyl)ethyl)benzothiazoloneHCID 69231068—

반응 단계

To a 100 ml round-bottomed flask with condenser and nitrogen inlet were added 1.0 gram (3.88 mmol) of 6-(2-bromoethyl)benzothiazolone, 822 mg (3.88 mmol) N-(1-naphthyl)piperazine, 410 mg (3.88 mmol) sodium carbonate, and 50 ml methylisobutlyketone. The reaction was refluxed for 24 hours, cooled, and evaporated. The residue was taken up in ethyl acetate, washed with water and brine, dried over sodium sulfate, and evaporated. The resulting solid was treated with hot ethyl acetate to afford a white solid, m.p. 198°-220° C., 540 mg (36%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06127373
출처 데이터셋uspto-grants-2000_10
ORD IDord-423c04872b3a492c8470d3dbbe872319
출처 메모uspto-grants-2000_10