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Sodium Azide → HCID 20810160, compound

HRID 1270343
Notes
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Reaction equation

HRID 1270343 reaction equation
N([O-])=O.[Na+].[NH2:5][C:6]1[CH:11]=[C:10]([F:12])[C:9]([N:13]2[CH2:18][CH2:17][C:16](=[O:19])[CH2:15][CH2:14]2)=[C:8]([F:20])[CH:7]=1.[N-:21]=[N+:22]=[N-].[Na+].C([O-])(=O)C.[Na+]>Cl>[N:5]([C:6]1[CH:11]=[C:10]([F:12])[C:9]([N:13]2[CH2:14][CH2:15][C:16](=[O:19])[CH2:17][CH2:18]2)=[C:8]([F:20])[CH:7]=1)=[N+:21]=[N-:22]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 33557Sodium AzideHCID 517045Sodium AcetateHCID 223856131-(4-Amino-2,6-difluorophenyl)-4-piperidinoneHCID 23668193Sodium Nitrite

Product 1

HCID 20810160HCID 20810160, compoundYield 55%

Reagents, catalysts & solvents 1

HCID 313
Hydrochloric Acid
Solvent

Conditions

Temperature
0 °C

Procedure

Sodium nitrite (2.40 g, 35.30 mmol) was added to an ice cooled solution of 1-(4-amino-2,6-difluorophenyl)-piperidin-4-one (4.00 g, 17.69 mmol), obtained in Preparation 17, in 6 N HCl (10 ml) and the resulting solution was stirred at 0° C. for 0.5 h. The reaction mixture was quenched with an aqueous solution of sodium azide (2.30 g, 35.3 mmol) and sodium acetate (29.0 g, 353 mmol). The reaction mixture was extracted with ethylacetate (100 ml×2) and the combined extract was washed with water followed by brine. The ethylacetate extract was dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by column chromatography (ethylacetate/pet ether; 1:9) to yield the title compound (2.20 g, 55%).

Workup

  1. extractionThe reaction mixture was extracted with ethylacetate (100 ml×2)
  2. extractionthe combined extract
  3. washwas washed with water
  4. extractionThe ethylacetate extract
  5. dry with materialwas dried over sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe resulting residue was purified by column chromatography (ethylacetate/pet ether; 1:9)

Sources & evidence

ORD record
ord-fa561680b5794fc3bb0a5022a3158ecf
Source dataset
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07202254B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes