Hydrochloric Acid → 2-[2-Fluoro-4-(4-pyrrolidin-1-yl-cyclohexyl)-phenyl]-2,8-diaza-spiro[4.5]decan-1-one hydrochloride
Reaction equation
[ClH:1].C(OC([N:9]1[CH2:37][CH2:36][C:12]2([C:16](=[O:17])[N:15]([C:18]3[CH:23]=[CH:22][C:21]([CH:24]4[CH2:29][CH2:28][CH:27]([N:30]5[CH2:34][CH2:33][CH2:32][CH2:31]5)[CH2:26][CH2:25]4)=[CH:20][C:19]=3[F:35])[CH2:14][CH2:13]2)[CH2:11][CH2:10]1)=O)(C)(C)C>O1CCOCC1>[ClH:1].[F:35][C:19]1[CH:20]=[C:21]([CH:24]2[CH2:29][CH2:28][CH:27]([N:30]3[CH2:34][CH2:33][CH2:32][CH2:31]3)[CH2:26][CH2:25]2)[CH:22]=[CH:23][C:18]=1[N:15]1[CH2:14][CH2:13][C:12]2([CH2:11][CH2:10][NH:9][CH2:37][CH2:36]2)[C:16]1=[O:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared in the same manner as Example 17 by using hydrochloric acid in dioxane to hydrolyze 2-[2-fluoro-4-(4-pyrrolidin-1-yl-cyclohexyl)-phenyl]-1-oxo-2,8-diaza-spiro[4.5]decane-8-carboxylic acid tert-butyl ester.
Sources & evidence
- ORD record
- ord-ddbff0d58ac246a0a033362e174020f0
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08735385B2
Reaction notes
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