Phenyl isocyanate → HCID 21101965, compound

HRID 1353361Notes

Reaction equation

HRID 1353361 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][CH:3]=1.[C:18]1([N:24]=[C:25]=[O:26])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.CCCCCC.CCOC(C)=O>C1COCC1>[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([N:12]3[CH2:17][CH2:16][N:15]([C:25]([NH:24][C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)=[O:26])[CH2:14][CH2:13]3)=[CH:7][CH:8]=[N:9]2)=[CH:4][CH:3]=1

Participants

5

Reactant 3

HCID 7672Phenyl isocyanateHCID 7383897-Chloro-4-(piperazin-1-yl)quinolineHCID 21226206Ethyl acetate hexane

Product 1

HCID 21101965HCID 21101965, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

7-Chloro-4-(piperazin-1-yl)quinoline (62 mg, 0.25 mmol) and phenyl isocyanate (33 μL, 0.30 mmol) in THF (10 mL) are reacted according to method C yielding the title product as colorless needles after column chromatography with hexane-EtOAc.

Sources & evidence

ORD record
ord-4c2251d2247448d78a496acaae00b0e9
Source dataset
uspto-grants-2007_05
Patent number
US07220856B2

Reaction notes

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