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Sodium Azide → HCID 89996091, 화합물

HRID 1480867
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HRID 1480867 반응식
S(OS(C(F)(F)F)(=O)=O)(C(F)(F)F)(=O)=O.[CH3:16][O:17][C:18]1[CH:19]=[C:20]([CH:25]=[CH:26][C:27]=1[N+:28]([O-:30])=[O:29])[C:21]([NH:23][CH3:24])=O.[N-:31]=[N+:32]=[N-:33].[Na+].C([O-])(O)=O.[Na+]>CC#N>[CH3:16][O:17][C:18]1[CH:19]=[C:20]([C:21]2[N:23]([CH3:24])[N:33]=[N:32][N:31]=2)[CH:25]=[CH:26][C:27]=1[N+:28]([O-:30])=[O:29]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 33557Sodium AzideHCID 67749Trifluoromethanesulfonic anhydrideHCID 516892Sodium BicarbonateHCID 568324173-Methoxy-N-methyl-4-nitrobenzamide

생성물 1

HCID 89996091HCID 89996091, 화합물수율 69.4%

시약·촉매·용매 1

HCID 6342Acetonitrile
용매

실험 절차

Triflic anhydride (0.27 mL, 1.580 mmol) was added dropwise to a solution of 3-methoxy-N-methyl-4-nitrobenzamide (Preparation 196, 0.166 g, 0.790 mmol) and sodium azide (0.205 g, 3.16 mmol) in MeCN (4.0 mL) at −10° C. The reaction mixture was warmed up to room temperature over 3 hours. The reaction was neutralised with saturated aqueous NaHCO3. The mixture was extracted with EtOAc and the organic layer washed with saturated aqueous NaHCO3, brine, dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by Biotage silica gel column chromatography eluting with cyclohexane/EtOAc 70/30 to 50/50 to afford the title compound as a white solid (129 mg, 69%).

후처리

  1. extractionThe mixture was extracted with EtOAc
  2. washthe organic layer washed with saturated aqueous NaHCO3, brine
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by Biotage silica gel column chromatography
  7. washeluting with cyclohexane/EtOAc 70/30 to 50/50

출처 및 근거

ORD 기록
ord-bd794829de96476a83ddb265f8667044
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409907B2

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