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Imidazole → 3-Bromo-6-(tert-butyldimethylsilyloxy)picolinonitrile

HRID 340198
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HRID 340198 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5](=[O:8])[NH:4][C:3]=1[C:9]#[N:10].[Si:11](Cl)([C:14]([CH3:17])([CH3:16])[CH3:15])([CH3:13])[CH3:12].N1C=CN=C1>CN(C=O)C.O>[Br:1][C:2]1[C:3]([C:9]#[N:10])=[N:4][C:5]([O:8][Si:11]([C:14]([CH3:17])([CH3:16])[CH3:15])([CH3:13])[CH3:12])=[CH:6][CH:7]=1
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참가 물질

6

반응물 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 668751023-Bromo-6-oxo-1,6-dihydropyridine-2-carbonitrile

생성물 1

HCID 668757543-Bromo-6-(tert-butyldimethylsilyloxy)picolinonitrile

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

실험 절차

A solution of 3-bromo-6-oxo-1,6-dihydropyridine-2-carbonitrile (from step 2) (1.0 eq.), tert-butyldimethylsilylchloride (TBSCl) (1.8 eq.), and imidazole (2.5 eq.) in DMF (0.2 M) was heated to 60° C. and stirred overnight. The reaction mixture was diluted with water and extracted with ether. The combined organic layers were dried over anhydrous MgSO4 and concentrated en vacuo. The residue was purified by a COMBIFLASH® system (ISCO) using 0-20% ethyl acetate in hexane to give 3-bromo-6-(tert-butyldimethylsilyloxy)picolinonitrile.

후처리

  1. extractionextracted with ether
  2. dry with materialThe combined organic layers were dried over anhydrous MgSO4
  3. concentrationconcentrated en vacuo
  4. customThe residue was purified by a COMBIFLASH® system (ISCO)

출처 및 근거

ORD 기록
ord-fadf6516f71b42049b6a7442dd297b70
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895577B2

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