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Water → 5-Bromo-2-(2H-tetrazol-5-yl)pyridine

HRID 1160189
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HRID 1160189 반응식
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([Br:9])=[CH:5][N:4]=1)#[N:2].[N-:10]=[N+:11]=[N-:12].[Na+].[Cl-].[NH4+].O>CN(C)C=O>[NH:10]1[C:1]([C:3]2[CH:8]=[CH:7][C:6]([Br:9])=[CH:5][N:4]=2)=[N:2][N:12]=[N:11]1
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참가 물질

6

반응물 4

HCID 962WaterHCID 25517Ammonium ChlorideHCID 33557Sodium AzideHCID 8171545-Bromopyridine-2-carbonitrile

생성물 1

HCID 234386835-Bromo-2-(2H-tetrazol-5-yl)pyridine수율 85%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
110 °C

실험 절차

10 g of 2-cyano-5-bromopyridine prepared in the Preparation example 5 was dissolved in 100 ml of dimethylformamide, 5.33 g of sodiumazide, and 4.4 g of ammonium chloride were added to the solution at room temperature, and the solution was stirred at the temperature of 110° C. for 3 hours for reaction. The reaction mixture was added with water and then was extracted with ethyl acetate. The organic layer, thus separated, was washed with brine, dehydrated, filtrated and concentrated in vacuo thereby to obtain 10.5 g of the title compound. Yield 85%.

후처리

  1. extractionwas extracted with ethyl acetate
  2. customThe organic layer, thus separated
  3. washwas washed with brine
  4. filtrationfiltrated
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-bf33a5f7539547dfa4ed1db167c346db
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07816379B2

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