Hydrochloric Acid → HCID 66589488, compound
Reaction equation
C(OC([NH:8][CH2:9][C:10]([O:12][C:13]1[CH:18]=[C:17]([NH:19][C:20]([NH:22][CH2:23][C:24]2[CH:25]=[C:26]3[C:30](=[CH:31][CH:32]=2)[C:29](=[O:33])[N:28]([CH:34]2[CH2:39][CH2:38][C:37](=[O:40])[NH:36][C:35]2=[O:41])[CH2:27]3)=[O:21])[CH:16]=[CH:15][C:14]=1[CH3:42])=[O:11])=O)(C)(C)C.[ClH:43]>C(Cl)Cl.CCOCC>[ClH:43].[NH2:8][CH2:9][C:10]([O:12][C:13]1[CH:18]=[C:17]([NH:19][C:20]([NH:22][CH2:23][C:24]2[CH:25]=[C:26]3[C:30](=[CH:31][CH:32]=2)[C:29](=[O:33])[N:28]([CH:34]2[CH2:39][CH2:38][C:37](=[O:40])[NH:36][C:35]2=[O:41])[CH2:27]3)=[O:21])[CH:16]=[CH:15][C:14]=1[CH3:42])=[O:11]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a mixture of 5-(3-((2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl)methyl)ureido)-2-methylphenyl 2-(tert-butoxycarbonylamino)acetate (0.58 g, 1.0 mmol) in DCM (50 mL) is added 2M HCl in ether (1 mL), and the mixture is stirred for 24 hrs. The solid precipitate is filtered, rinsed with DCM (10 mL), and dried under vacuum to provide the product.
Workup
- filtrationThe solid precipitate is filtered
- washrinsed with DCM (10 mL)
- customdried under vacuum
- customto provide the product
Sources & evidence
- ORD record
- ord-752ab74b2ae9495e8b01c107a13baeed
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09227954B2
Reaction notes
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