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

HRID 340198
ノート
印刷プレビュー

反応式

HRID 340198 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-fadf6516f71b42049b6a7442dd297b70
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08895577B2

反応ノート

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