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1H-Pyrazole-4-carbonitrile → 1-(3-bromo-2-formylphenyl)-1H-pyrazole-4-carbonitrile

HRID 1025613
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HRID 1025613 반응식
[NH:1]1[CH:5]=[C:4]([C:6]#[N:7])[CH:3]=[N:2]1.CC(C)([O-])C.[K+].[Br:14][C:15]1[CH:22]=[CH:21][CH:20]=[C:19](F)[C:16]=1[CH:17]=[O:18]>CS(C)=O>[Br:14][C:15]1[C:16]([CH:17]=[O:18])=[C:19]([N:1]2[CH:5]=[C:4]([C:6]#[N:7])[CH:3]=[N:2]2)[CH:20]=[CH:21][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 5644491H-Pyrazole-4-carbonitrileHCID 224739772-Bromo-6-fluorobenzaldehydeHCID 23665647Potassium tert-butoxide

생성물 1

HCID 866737221-(3-bromo-2-formylphenyl)-1H-pyrazole-4-carbonitrile수율 55.4%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

1H-pyrazole-4-carbonitrile (935 mg, 10.0 mmol, Eq: 1.00) was dissolved in 15 mL of dry DMSO and potassium tert-butoxide (1.19 g, 10.0 mmol, Eq: 1.00) was added. The mixture was stirred at room temperature for 20 minutes and 2-bromo-6-fluorobenzaldehyde (4.08 g, 20.1 mmol, Eq: 2) was added. The mixture was stirred at room temperature overnight and then extracted with ethyl acetate and water. The organic layer was dried and concentrated. The crude material was purified by flash chromatography (silica gel, 40 g, 20% to 40% EtOAc in hexanes) to give 1-(3-bromo-2-formylphenyl)-1H-pyrazole-4-carbonitrile (1.53 g, 55%).

후처리

  1. stirringThe mixture was stirred at room temperature overnight
  2. extractionextracted with ethyl acetate and water
  3. customThe organic layer was dried
  4. concentrationconcentrated
  5. customThe crude material was purified by flash chromatography (silica gel, 40 g, 20% to 40% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-1b1df8405c7e4ab285cb26745765008d
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08729078B2

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