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Sodium Azide → HCID 20810160, 화합물

HRID 1270343
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HRID 1270343 반응식
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]
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6

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

생성물 1

HCID 20810160HCID 20810160, 화합물수율 55%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

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온도
0 °C

실험 절차

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%).

후처리

  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)

출처 및 근거

ORD 기록
ord-fa561680b5794fc3bb0a5022a3158ecf
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07202254B2

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