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Phosphorus oxychloride → 2-(5-bromopyridine-3-yl)-1-phenyl-1H-benzimidazole

HRID 520824
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HRID 520824 반응식
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH:23]=1)[C:7]([NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[NH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=O.P(Cl)(Cl)(Cl)=O>O1CCOCC1>[Br:1][C:2]1[CH:23]=[C:6]([C:7]2[N:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=3[N:9]=2)[CH:5]=[N:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 706542275-bromo-N-(2-(phenylamino)phenyl)nicotinamide

생성물 1

HCID 230940852-(5-bromopyridine-3-yl)-1-phenyl-1H-benzimidazole수율 89%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
100 °C

실험 절차

Compound 1E (20.0 g, 54.3 mmol) was dissolved in 1,4-dioxane (anhydrous, 150 mL). Phosphorous oxychloride (36 g, 235 mmol) was then added dropwise. The resulting solution was heated at about 100° C. overnight; solids formed. After cooling to RT, the mixture was poured into hexanes (250 mL) to form additional precipitate. Solids were filtered then redissolved in DCM (200 mL) and washed with potassium carbonate (200 mL, saturated solution). The organic phase was collected, dried over sodium sulfate, and loaded onto silica gel. Short silica plug (20% ethyl acetate in hexanes and precipitation from hexanes gave 16.86 g of Compound 1F; 89% yield, pure by HNMR.

후처리

  1. customsolids formed
  2. temperatureAfter cooling to RT
  3. customto form additional precipitate
  4. filtrationSolids were filtered
  5. dissolutionthen redissolved in DCM (200 mL)
  6. washwashed with potassium carbonate (200 mL, saturated solution)
  7. customThe organic phase was collected
  8. dry with materialdried over sodium sulfate
  9. customShort silica plug (20% ethyl acetate in hexanes and precipitation from hexanes

출처 및 근거

ORD 기록
ord-20b39a85af3e49d2ae7fa92bd31b5f13
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09328094B2

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