1-Piperazinyl(4-((7-(trifluoromethyl)-4-quinolinyl)amino)phenyl)methanone → HCID 20392866, compound

HRID 1863018Notes

Reaction equation

HRID 1863018 reaction equation
[F:1][C:2]([F:29])([F:28])[C:3]1[CH:12]=[C:11]2[C:6]([C:7]([NH:13][C:14]3[CH:27]=[CH:26][C:17]([C:18]([N:20]4[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]4)=[O:19])=[CH:16][CH:15]=3)=[CH:8][CH:9]=[N:10]2)=[CH:5][CH:4]=1.[CH2:30]([N:32]([CH2:37][CH3:38])[S:33](Cl)(=[O:35])=[O:34])[CH3:31]>C(N(CC)CC)C>[CH2:30]([N:32]([CH2:37][CH3:38])[S:33]([N:23]1[CH2:24][CH2:25][N:20]([C:18](=[O:19])[C:17]2[CH:26]=[CH:27][C:14]([NH:13][C:7]3[C:6]4[C:11](=[CH:12][C:3]([C:2]([F:1])([F:28])[F:29])=[CH:4][CH:5]=4)[N:10]=[CH:9][CH:8]=3)=[CH:15][CH:16]=2)[CH2:21][CH2:22]1)(=[O:35])=[O:34])[CH3:31]

Participants

4

Reactant 2

HCID 30552431-Piperazinyl(4-((7-(trifluoromethyl)-4-quinolinyl)amino)phenyl)methanoneHCID 11252267N,N-diethylsulfamoyl chloride

Product 1

HCID 20392866HCID 20392866, compound

Reagents, catalysts & solvents 1

HCID 8471TriethylamineSolvent

Procedure

In the manner given in Example 14, 4-[4-[[7-(trifluoromethyl)-4-quinolinyl]amino]benzoyl]piperazine is reacted with diethylsulfamoyl chloride, in the presence of triethylamine to give 1-[(diethylamino)sulfonyl]-4-[4-[[7-(trifluoromethyl)-4-quinolinyl]amino]benzoyl]piperazine.

Sources & evidence

ORD record
ord-0c0d62a9364c4ab2b43c90a44d8b7c56
Source dataset
uspto-grants-1979_09
Patent number
US04167567

Reaction notes

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