Hydrochloride methanol → 2-(1-(2-Hydroxyethyl)-2,6-dioxopiperidin-3-yl)isoindolin-1,3-dione 2-(diethylamino)acetate hydrochloride
Reaction equation
[CH2:1]([N:3]([CH2:8][CH3:9])[CH2:4][C:5]([OH:7])=[O:6])[CH3:2].[OH:10][CH2:11][CH2:12][N:13]1[C:18](=[O:19])[CH2:17][CH2:16][CH:15]([N:20]2[C:28](=[O:29])[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[C:21]2=[O:30])[C:14]1=[O:31].[ClH:32].CO>C(Cl)Cl>[ClH:32].[CH2:1]([N:3]([CH2:8][CH3:9])[CH2:4][C:5]([OH:7])=[O:6])[CH3:2].[OH:10][CH2:11][CH2:12][N:13]1[C:18](=[O:19])[CH2:17][CH2:16][CH:15]([N:20]2[C:21](=[O:30])[C:22]3[C:27](=[CH:26][CH:25]=[CH:24][CH:23]=3)[C:28]2=[O:29])[C:14]1=[O:31]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound obtained from example 9 (76 mg) was dissolved in DCM (10 mL), and 15% HCl/methanol solution (10 mL) was added dropwise. The solvent was removed by rotary evaporation in vacuo to afford white solid (80 mg). Solubility of this compound in water was higher than 100 mg/mL.
Workup
- customThe solvent was removed by rotary evaporation in vacuo
Sources & evidence
- ORD record
- ord-751c84fc087a485eb3cd4af688792f38
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08637545B2
Reaction notes
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