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Methyl iodide → 3-Bromo-6-methoxypicolinonitrile

HRID 1479485
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HRID 1479485 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5](=[O:8])[NH:4][C:3]=1[C:9]#[N:10].I[CH3:12]>C1(C)C=CC=CC=1.C(=O)([O-])[O-].[Ag+2]>[Br:1][C:2]1[C:3]([C:9]#[N:10])=[N:4][C:5]([O:8][CH3:12])=[CH:6][CH:7]=1
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참가 물질

5

반응물 2

HCID 6328Methyl iodideHCID 668751023-Bromo-6-oxo-1,6-dihydropyridine-2-carbonitrile

생성물 1

HCID 534856273-Bromo-6-methoxypicolinonitrile

시약·촉매·용매 2

HCID 178418647HCID 178418647, 화합물촉매HCID 1140Toluene용매

실험 절차

A solution of 3-bromo-6-oxo-1,6-dihydropyridine-2-carbonitrile (from Example 15/Step 2) (1.0 eq.), silver carbonate (1.3 eq.), and iodomethane (1.2 eq.) in toluene (0.2 M) was stirred in the dark at room temperature overnight. The solvent was concentrated en vacuo, and the resulting residue was purified by a COMBIFLASH® system (ISCO) using 0-80% ethyl acetate in hexane to give 3-bromo-6-methoxypicolinonitrile.

후처리

  1. customdark at room temperature
  2. customovernight
  3. concentrationThe solvent was concentrated en vacuo
  4. customthe resulting residue was purified by a COMBIFLASH® system (ISCO)

출처 및 근거

ORD 기록
ord-e3e696424e214f24b0cf2023ebf5f8aa
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09408907B2

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