Potassium Carbonate → dimethyl 2-bromo-1-(but-2-ynyl)-1H-imidazole-4,5-dicarboxylate

HRID 2113477노트

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HRID 2113477 반응식
Br[CH2:2][C:3]#[C:4][CH3:5].[Br:6][C:7]1[NH:8][C:9]([C:16]([O:18][CH3:19])=[O:17])=[C:10]([C:12]([O:14][CH3:15])=[O:13])[N:11]=1.C(=O)([O-])[O-].[K+].[K+].S([O-])([O-])(=O)=S.[Na+].[Na+]>CN(C)C=O>[Br:6][C:7]1[N:11]([CH2:2][C:3]#[C:4][CH3:5])[C:10]([C:12]([O:14][CH3:15])=[O:13])=[C:9]([C:16]([O:18][CH3:19])=[O:17])[N:8]=1

참가 물질

6

실험 절차

3.06 g 1-bromo-2-butyne are added dropwise to a mixture of 6.00 g of dimethyl 2-bromo-1H-imidazole-4,5-dicarboxylate and 3.80 g of potassium carbonate in 40 ml of dimethylformamide. The mixture is stirred for 12 h at ambient temperature and then added to an aqueous saturated solution of sodium thiosulphate. The organic phase is separated off and the aqueous phase is extracted three times with ethyl acetate. The combined organic phases are dried over sodium sulphate, the solvent is removed and the residue is chromatographed over silica gel (cyclohexane/ethyl acetate 4:1>1:1).

후처리

  1. customThe organic phase is separated off
  2. extractionthe aqueous phase is extracted three times with ethyl acetate
  3. dry with materialThe combined organic phases are dried over sodium sulphate
  4. customthe solvent is removed
  5. customthe residue is chromatographed over silica gel (cyclohexane/ethyl acetate 4:1>1:1)

출처 및 근거

ORD 기록
ord-0b3c97df53334c5eb4328ea70f511474
출처 데이터셋
uspto-grants-2008_10
특허 번호
US07432262B2

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