Hydrogen Peroxide → HCID 67141825, compound
Reaction equation
OO.[ClH:3].[CH2:4]([N:7]1[C:11]2=[C:12]([N:16]3[CH2:25][CH2:24][C:23]4[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=4)[CH2:17]3)[N:13]=[CH:14][CH:15]=[C:10]2[C:9]([S:26][CH3:27])=[C:8]1[CH3:28])[CH:5]=[CH2:6].S([O-])([O-])(=[O:31])=S.[Na+].[Na+].C(=O)([O-])[O-].[K+].[K+]>C(O)(=O)C>[ClH:3].[CH2:4]([N:7]1[C:11]2=[C:12]([N:16]3[CH2:25][CH2:24][C:23]4[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=4)[CH2:17]3)[N:13]=[CH:14][CH:15]=[C:10]2[C:9]([S:26]([CH3:27])=[O:31])=[C:8]1[CH3:28])[CH:5]=[CH2:6]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Hydrogen peroxide (50 wt. %, 100 μl) was added to a solution of 2-(1-allyl-2-methyl-3-methylsulfanyl-1H-pyrrolo[2,3-c]pyridin-7-yl)-1,2,3,4-tetrahydroisoquinoline hydrochloride (45 mg, 0.12 mmol) prepared in Example 631 in acetic acid (3 ml). The reaction mixture was stirred for 30 minutes at room temperature and sodium thiosulfate was added thereto. The reaction mixture was basified with a potassium carbonate solution and then extracted with dichloromethane. The organic layer was dried on anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was dissolved in ethyl ether, saturated with hydrochloric acid gas, and then filtered to give 5.5 mg of the titled compound as a white solid.
Workup
- extractionextracted with dichloromethane
- dry with materialThe organic layer was dried on anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
- dissolutionThe resulting residue was dissolved in ethyl ether, saturated with hydrochloric acid gas
- filtrationfiltered
Sources & evidence
- ORD record
- ord-92f7b7828c014f4fa5be35d796e969a9
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08188114B2
Reaction notes
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