Sodium Hydroxide → 5-Allyl-1-benzyl-6-hydroxy-4-(4-isopropyl-phenyl)-1H-quinazolin-2-one
Reaction equation
[CH2:1]([C:4]1[C:9]([OH:10])=[CH:8][CH:7]=[C:6]([NH:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:5]=1[C:19]([C:21]1[CH:26]=[CH:25][C:24]([CH:27]([CH3:29])[CH3:28])=[CH:23][CH:22]=1)=O)[CH:2]=[CH2:3].[O-:30][C:31]#[N:32].[Na+].[OH-].[Na+]>C(O)(=O)C>[CH2:1]([C:4]1[C:9]([OH:10])=[CH:8][CH:7]=[C:6]2[C:5]=1[C:19]([C:21]1[CH:26]=[CH:25][C:24]([CH:27]([CH3:29])[CH3:28])=[CH:23][CH:22]=1)=[N:32][C:31](=[O:30])[N:11]2[CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[CH:2]=[CH2:3]Participants
5
Procedure
A solution of 15 mg (39 μmol) (2-allyl-6-benzylamino-3-hydroxy-phenyl)-(4-isopropyl-phenyl)-methanone and 2.5 mg sodium cyanate in 0.2 ml acetic acid is stirred at r.t. for 16 h. Aqueous sodium hydroxide solution is added and the product is extracted with dichloromethane.
Workup
- extractionthe product is extracted with dichloromethane
Sources & evidence
- ORD record
- ord-3417843fbeca43efb9a8cb45fada7b44
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696216B2
Reaction notes
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