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Acridone → 9(10H)-Acridinone, 10-(2-(dimethylamino)ethyl)-

HRID 986252
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인쇄 미리보기

반응식

HRID 986252 반응식
[CH:1]1[C:14]2[C:13](=[O:15])[C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[NH:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[H-].[Na+].Cl.Cl[CH2:20][CH2:21][N:22]([CH3:24])[CH3:23]>CN(C)C=O>[CH3:23][N:22]([CH3:24])[CH2:21][CH2:20][N:6]1[C:5]2[C:14](=[CH:1][CH:2]=[CH:3][CH:4]=2)[C:13](=[O:15])[C:12]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]1=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 2015AcridoneHCID 24758Sodium hydrideHCID 11636816N,N-Dimethylaminoethyl chloride hydrochloride

생성물 1

HCID 30147319(10H)-Acridinone, 10-(2-(dimethylamino)ethyl)-

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 3.9 g of acridanone, 1.0 g of sodium hydride and 80 ml of dimethylformamide is stirred for 0.5 hours, then treated with 2.9 g of 1-chloro-2-dimethylaminoethane hydrochloride, stirred at 60° for 18 hours and evaporated. The residue is extracted with methylene chloride. The extract is washed with water, dried over sodium sulfate and evaporated. By crystallization from isopropyl ether there is obtained 10-[2-(dimethylamino)ethyl]-9-acridanone of melting point 145°-146°.

후처리

  1. stirringstirred at 60° for 18 hours
  2. customevaporated
  3. extractionThe residue is extracted with methylene chloride
  4. washThe extract is washed with water
  5. dry with materialdried over sodium sulfate
  6. customevaporated
  7. customBy crystallization from isopropyl ether

출처 및 근거

ORD 기록
ord-e299d4cefb744a1a8a691b151273059b
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04711889

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