Nitric Acid → HCID 178440254, compound

HRID 1749262Notes

Reaction equation

HRID 1749262 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

6

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: 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

  1. temperaturecooled with ice at 5° C. or below
  2. stirringsubsequently kept stirred at room temperature (20-30° C.) overnight
  3. additionThe reaction mixture was poured into ice
  4. extractionThe mixture was extracted twice with chloroform
  5. concentrationthe organic layer was concentrated under reduced pressure
  6. customThe resulting residue was purified by silica gel column chromatography (methylene chloride:methanol=50:1 to 10:1)

Sources & evidence

ORD record
ord-1239c4caf3b24cdb94dfa975503127d3
Source dataset
uspto-grants-2015_10
Patent number
US09156817B2

Reaction notes

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