Sodium Hydroxide → HCID 21928838, compound
Reaction equation
[C:1]1([C:7]2([C:35]3[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=3)[CH2:15][C:14]3[N:13](S(C4C=CC(C)=CC=4)(=O)=O)[N:12]=[C:11]([NH:26][C:27](=[O:34])[C:28]4[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=4)[C:10]=3[CH:9]=[CH:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>O1CCCC1>[C:35]1([C:7]2([C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)[CH2:15][C:14]3[NH:13][N:12]=[C:11]([NH:26][C:27](=[O:34])[C:28]4[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=4)[C:10]=3[CH:9]=[CH:8]2)[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
But starting with 0.14 g of N-[6,6-diphenyl-1-(4-toluenesulphonyl)-6,7-dihydro-1H-indazol-3-yl)benzamide and 0.78 cm3 of aqueous 1N sodium hydroxide solution in 10 cm3 of tetrahydrofuran. 0.27 g of N-(6,6-diphenyl-6,7-dihydro-1H-indazol-3-yl)benzamide is thus obtained in the form of a solid, the characteristics of which are as follows:
Sources & evidence
- ORD record
- ord-f945882c4e1a40f2a52211ba955b7e41
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07119115B2
Reaction notes
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