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Phosphorus oxychloride → 4,6-Dichloro-3-nitroquinoline

HRID 1672316
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HRID 1672316 반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][C:6]([N+:12]([O-:14])=[O:13])=[C:5]2O.O=P(Cl)(Cl)[Cl:18]>>[Cl:18][C:5]1[C:4]2[C:9](=[CH:10][CH:11]=[C:2]([Cl:1])[CH:3]=2)[N:8]=[CH:7][C:6]=1[N+:12]([O-:14])=[O:13]
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참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178526764HCID 178526764, 화합물

생성물 1

HCID 106816704,6-Dichloro-3-nitroquinoline

실험 절차

11 g (48.97 mmol) 6-chloro-3-nitro-quinolin-4-ol (Example 23b) in 80 ml POCl3 are heated and kept under reflux for 5 h (tlc-control). The cool reaction mixture is poured slowly into 1.5 l ice-water. The title compound separates as a solid. The mixture is stirred for 15 min. the temperature not exceeding 0-5° C. The solid is filtered off, washed with water and dissolved in 200 ml ethylacetate. The organic phase is washed with a mixture of 200 ml water and 38 ml 2N sodium hydroxide solution and again water. After drying over MgSO4, the solvent is evaporated almost to dryness; to the residue hexane is added and the product is isolated by filtration as a dark-grey powder. This material is used in the next step without further purification. mp: 118-120° C.; NMR (DMSO-d6): 9.43/s (1H); 8.43/d (1H), 8.25/d (1H), 8.10/d×d (1H); HPLC: tret=12.84 min (Grad 1).

후처리

  1. temperatureunder reflux for 5 h (tlc-control)
  • customThe cool reaction mixture
  • 출처 및 근거

    ORD 기록
    ord-2683920b43c94d3097d7f1d959fe1b97
    출처 데이터셋
    uspto-grants-2011_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07998972B2

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