Phenylsulphonyl isocyanate → HCID 178452697, compound
Reaction equation
[Cl:1][C:2]1[CH:11]=[C:10]([Cl:12])[CH:9]=[C:8]2[C:3]=1[C:4](=O)[CH:5]=[C:6]([C:13](=[O:28])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[NH:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[NH:7]2.[C:30]1([S:36]([N:39]=C=O)(=[O:38])=[O:37])[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>C(#N)C>[Cl:1][C:2]1[CH:11]=[C:10]([Cl:12])[CH:9]=[C:8]2[C:3]=1[C:4](=[N:39][S:36]([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)(=[O:38])=[O:37])[CH:5]=[C:6]([C:13](=[O:28])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[NH:20][C:21]([O:23][C:24]([CH3:25])([CH3:26])[CH3:27])=[O:22])[NH:7]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Combine 5,7-dichloro-2-[2-(t-butoxycarbonylamino) benzoyl]-1,4-dihydroquinol-4-one (2 mmol) and benzenesulfonyl isocyanate (2.2 mmol) in acetonitrile (9 mL) and heat at reflux for 48 hours. Add methanol (5 mL) to quench the reaction. Evaporate in vacuo to obtain a residue. Chromatograph the residue on a column of silica gel to give the title compound.
Workup
- temperatureat reflux for 48 hours
- customAdd methanol (5 mL) to quench
- customthe reaction
- customEvaporate in vacuo
- customto obtain a residue
Sources & evidence
- ORD record
- ord-f257df69fd414b46bdddd8457a8cf9ea
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05684017
Reaction notes
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