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Hydrochloric Acid → p-[(7-trifluoromethyl-4-quinolyl)amino]-N,N-dimethylbenzamide

HRID 2398726
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HRID 2398726 반응식
[CH3:1][N:2]([CH3:12])[C:3](=[O:11])[C:4]1[CH:9]=[CH:8][C:7]([NH2:10])=[CH:6][CH:5]=1.Cl[C:14]1[C:23]2[C:18](=[CH:19][C:20]([C:24]([F:27])([F:26])[F:25])=[CH:21][CH:22]=2)[N:17]=[CH:16][CH:15]=1.Cl.[OH-].[Na+]>C(O)C>[F:27][C:24]([F:25])([F:26])[C:20]1[CH:19]=[C:18]2[C:23]([C:14]([NH:10][C:7]3[CH:8]=[CH:9][C:4]([C:3]([N:2]([CH3:12])[CH3:1])=[O:11])=[CH:5][CH:6]=3)=[CH:15][CH:16]=[N:17]2)=[CH:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 676684-Chloro-7-(trifluoromethyl)quinolineHCID 2355274-Amino-N,N-dimethylbenzamide

생성물 1

HCID 21433867p-[(7-trifluoromethyl-4-quinolyl)amino]-N,N-dimethylbenzamide

시약·촉매·용매 1

HCID 702Ethanol
용매

실험 절차

A mixture of 0.1 mole of N,N-dimethyl-p-aminobenzamide, 0.1 mole of 4-chloro-7-trifluoromethylquinoline, 8 ml. of concentrated hydrochloric acid and 500 ml. of absolute ethanol is heated at reflux for 19 hours, after which 100 ml. of 2.5N sodium hydroxide is added. The mixture is cooled and filtered and the filter cake is recrystallized from methanol. There is thus obtained p-[(7-trifluoromethyl-4-quinolyl)amino]-N,N-dimethylbenzamide.

후처리

  1. temperatureat reflux for 19 hours
  2. temperatureThe mixture is cooled
  3. filtrationfiltered
  4. customthe filter cake is recrystallized from methanol

출처 및 근거

ORD 기록
ord-571c6d3402fc4c39a9d1a70b7c14419a
출처 데이터셋
uspto-grants-1977_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04025629

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