Nitric Acid → HCID 178440254, compound
Reaction equation
[CH:1]([C:4]1[CH:9]=[C:8]([CH:10]([CH3:12])[CH3:11])[N:7]=[C:6]([OH:13])[N:5]=1)([CH3:3])[CH3:2].S(=O)(=O)(O)O.[N+:19]([O-])([OH:21])=[O:20].[OH-].[Na+]>C(Cl)(Cl)Cl>[CH:10]([C:8]1[C:9]([N+:19]([O-:21])=[O:20])=[C:4]([CH:1]([CH3:3])[CH3:2])[N:5]=[C:6]([OH:13])[N:7]=1)([CH3:12])[CH3:11]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 25 °C
Procedure
Compound 4 (20 mg) was suspended in a mixture of concentrated sulfuric acid (1 mL) and chloroform (1 mL). To the resulting mixture, fuming nitric acid (166 μL: d=1.50) was added while being stirred and cooled with ice at 5° C. or below. The resulting mixture was allowed to slowly warm to room temperature (20-30° C.), and subsequently kept stirred at room temperature (20-30° C.) overnight. The reaction mixture was poured into ice and neutralized with a 10N aqueous sodium hydroxide solution to a pH of approx. 5 (at 20° C. or below). The mixture was extracted twice with chloroform and the organic layer was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (methylene chloride:methanol=50:1 to 10:1) to give 17.8 mg (49% yield) of the desired product as a brown amorphous.
Workup
- temperaturecooled with ice at 5° C. or below
- stirringsubsequently kept stirred at room temperature (20-30° C.) overnight
- additionThe reaction mixture was poured into ice
- extractionThe mixture was extracted twice with chloroform
- concentrationthe organic layer was concentrated under reduced pressure
- customThe resulting residue was purified by silica gel column chromatography (methylene chloride:methanol=50:1 to 10:1)
Sources & evidence
- ORD record
- ord-371cc5a96db3436a9286d75d310daca5
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09139559B2
Reaction notes
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