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Phosphorus oxychloride → 4-Chloro-6-nitro-1,8-naphthyridine-3-carbonitrile

HRID 276829
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HRID 276829 반응식
[N+:1]([C:4]1[CH:5]=[C:6]2[C:11](=[N:12][CH:13]=1)[NH:10][CH:9]=[C:8]([C:14]#[N:15])[C:7]2=O)([O-:3])=[O:2].P(Cl)(Cl)([Cl:19])=O>>[Cl:19][C:7]1[C:6]2[C:11](=[N:12][CH:13]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)[N:10]=[CH:9][C:8]=1[C:14]#[N:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 185489504-Hydroxy-6-nitro-1,8-naphthyridine-3-carbonitrile

생성물 1

HCID 155506564-Chloro-6-nitro-1,8-naphthyridine-3-carbonitrile

실험 절차

A mixture of 19.3 g (89.3 mmol) of 6-nitro-4-oxo-1,4-dihydro-[1.8]naphthyridine-3-carbonitrile in 386 ml of phosphorous oxychloride was refluxed for 24 hr. Excess phosphorous oxychloride was removed. The residue is mixed with ethyl acetate and 15 g of potassium hydroxide in 200 ml of ice water. The organic layer was separated and the aqueous layer was extract several more times with ethyl acetate. The combined volume of extracts was 4000 ml. The extracts were dried of magnesium sulfate and the solution was filter through a short silica gel column. The solvent was removed. The residue was stirred with ether and the solid was collected giving 15.7 g of the title compound as an orange solid: mass spectrum (electrospray, m/e): M+H 235.

후처리

  1. temperature
was refluxed for 24 hr
  • customExcess phosphorous oxychloride was removed
  • additionThe residue is mixed with ethyl acetate and 15 g of potassium hydroxide in 200 ml of ice water
  • customThe organic layer was separated
  • extractionthe aqueous layer was extract several more times with ethyl acetate
  • dry with materialThe extracts were dried of magnesium sulfate
  • filtrationthe solution was filter through a short silica gel column
  • customThe solvent was removed
  • customthe solid was collected
  • 출처 및 근거

    ORD 기록
    ord-6be5ba88c19546a79860c154b3af064b
    출처 데이터셋
    uspto-grants-2002_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06355636B1

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