4-Fluorophenyl isocyanate → HCID 21101811, compound
Reaction equation
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([N:12]3[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]3)=[CH:7][CH:8]=[N:9]2)=[CH:4][C:3]=1[F:18].[F:19][C:20]1[CH:25]=[CH:24][C:23]([N:26]=[C:27]=[O:28])=[CH:22][CH:21]=1.CCCCCC.CCOC(C)=O>C1COCC1>[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([N:12]3[CH2:13][CH2:14][N:15]([C:27]([NH:26][C:23]4[CH:24]=[CH:25][C:20]([F:19])=[CH:21][CH:22]=4)=[O:28])[CH2:16][CH2:17]3)=[CH:7][CH:8]=[N:9]2)=[CH:4][C:3]=1[F:18]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
7-Chloro-6-fluoro-4-(piperazin-1-yl)quinoline (0.36 g, 1.35 mmol) and 4-fluorophenyl isocyanate (171 μL, 1.5 mmol) in THF (10 mL) are reacted according to method C yielding the product as a colorless solid after column chromatography with hexane-EtOAc.
Sources & evidence
- ORD record
- ord-8a77006744624aff88cfc19e2e1190e8
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07220856B2
Reaction notes
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