Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 522937생성일: 2026년 10월 25일
1,5-Dichloroanthraquinone → 1-Chloro-5-(2-(dimethylamino)ethylamino)anthracene-9,10-dione
https://huagongshe.com/reaction/522937
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,5-Dichloroanthraquinone | HCID 6711 | — |
| 반응물 | N,N-Dimethylethylenediamine | HCID 66053 | — |
| 용매 | Dimethylacetamide | HCID 31374 | — |
| 생성물 | 1-Chloro-5-(2-(dimethylamino)ethylamino)anthracene-9,10-dione | HCID 14320125 | 16.9% |
반응 단계
A mixture of 1,5-dichloro anthraquinone (5.0 g, 18.0 mmol), N,N-dimethylacetamide (30 mL) and N,N-dimethylethylenediamine (2 mL, 18 mmol) was stirred at room temperature for 1 hour and then heated in an oil bath (T=100° C.) for 45 minutes. Reaction mixture was cooled and filtered. To the filtrate petroleum ether (50 mL) was added and combined mixture was stirred at 4° C. over night. Precipitated solid was removed by filtration and supernatant was evaporated to dryness, co-evaporated with chloroform and dried under vacuum. The crude dye was then purified on Biotage SP4 system using a gradient of methanol in chloroform. Appropriate fractions were combined and evaporated to dryness to provide Compound 17 (1.0 g) as a red solid. Rf (9:1 CHCl3/MeOH): 0.46; Abs (max, PBS)=500 nm. The structure of Compound 17 is given below:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US09334281B2 |
|---|
| 출처 데이터셋 | uspto-grants-2016_05 |
|---|
| ORD ID | ord-16fd1327c7c2454691174437859f1ca9 |
|---|
| 출처 메모 | uspto-grants-2016_05 |
|---|