Hydrochloric Acid → HCID 46234399, compound
Reaction equation
[CH3:1][C:2]1[O:3][C:4]([CH3:36])=[CH:5][C:6]=1[C:7]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:24]=[C:23]3[C:19]([C:20]([C:25]([NH:27][CH2:28][CH2:29][N:30]4[CH2:35][CH2:34][O:33][CH2:32][CH2:31]4)=[O:26])=[N:21][NH:22]3)=[CH:18][CH:17]=2)=[CH:12][CH:11]=1)=[O:8].[ClH:37]>O1CCCC1.O1CCOCC1>[ClH:37].[CH3:1][C:2]1[O:3][C:4]([CH3:36])=[CH:5][C:6]=1[C:7]([NH:9][C:10]1[CH:11]=[CH:12][C:13]([C:16]2[CH:24]=[C:23]3[C:19]([C:20]([C:25]([NH:27][CH2:28][CH2:29][N:30]4[CH2:35][CH2:34][O:33][CH2:32][CH2:31]4)=[O:26])=[N:21][NH:22]3)=[CH:18][CH:17]=2)=[CH:14][CH:15]=1)=[O:8]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a stirred solution of 6-(4-(2,5-dimethylfuran-3-carboxamido)phenyl)-N-(2-morpholinoethyl)-1H-indazole-3-carboxamide (38 mg, 78 umol) in tetrahydrofuran (1 Ml), 4N hydrochloric acid solution in dioxane (20 μl) was added at room temperature. After 30 min, the resulting solid was filtered and dried to give 6-(4-(2,5-dimethylfuran-3-carboxamido)phenyl)-N-(2-morpholinoethyl)-1H-indazole-3-carboxamide hydrochloride (35 mg).
Workup
- filtrationthe resulting solid was filtered
- customdried
Sources & evidence
- ORD record
- ord-5207bbe70c344d17ae2a2931f534ff3e
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08754209B2
Reaction notes
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