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HRID 71020생성일: 2026년 10월 24일

Ethanol → (Imidazo[2,1-b]benzothiazol-2-yl)aniline

https://huagongshe.com/ko/reaction/71020

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참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물WaterHCID 962—
반응물Sulfuric AcidHCID 1118—
반응물Benzo(d)thiazol-2-amineHCID 8706—
반응물2-Bromo-4'-nitroacetophenoneHCID 66840—
촉매IronHCID 23925—
생성물(Imidazo[2,1-b]benzothiazol-2-yl)anilineHCID 66592992—

반응 조건

온도0 °C

반응 단계

A mixture of 2-aminobenzothiazole (4.00 g, 26.6 mmol) and 2-bromo-4′-nitroacetophenone (7.32 g, 30.0 mmol) was refluxed in ethanol for 90 min and then the mixture was cooled to 0° C. The solid (about 2 g) was collected by filtration, washed with the minimum quantity of cold ethanol and then dissolved again in 150 ml of ethanol and added of iron powder (7.47 g, 133.75 mmol), water (30 ml) and H2SO4 12N (750 μl). The mixture was stirred at 90° C. for 1 h, then filtered on celite and washed with hot ethanol. The solvent was removed under reduced pressure and the crude material was treated with aqueous NaHCO3 (10%, 400 ml) and extracted with CH2Cl2 (3×150 ml). The organic phase was dried with anhydrous Na2SO4 and the solvent removed under reduced pressure to afford 4-[(imidazo[2,1-b]benzothiazol-2-yl)aniline.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822698B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-5cb9c0d62efe480bb4d5d681b4e59ec7
출처 메모uspto-grants-2014_09