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Lawesson's reagent → HCID 178425914, 화합물

HRID 570981
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HRID 570981 반응식
[CH3:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[CH:4][C:3]=1[C:11]#[C:12][C:13]1[CH:14]=[N:15][C:16]2[C:21]([CH:22]=1)=[CH:20][CH:19]=[CH:18][CH:17]=2.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:32])=CC=1>C1COCC1>[CH3:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:7])=[S:32])=[CH:4][C:3]=1[C:11]#[C:12][C:13]1[CH:14]=[N:15][C:16]2[C:21]([CH:22]=1)=[CH:20][CH:19]=[CH:18][CH:17]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 87949Lawesson's reagentHCID 70557832HCID 70557832, 화합물

생성물 1

HCID 178425914HCID 178425914, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 4-methyl-3-[(quinolin-3-yl)ethynyl]benzoic acid (0.3 g, 1.3 mmol) and Lawesson's reagent (0.5 ml, 1.3 mmol) in THF (10 ml) was stirred at ambient temperature for 1 hr under an atmosphere of nitrogen. The reaction mixture was concentrated and the crude product was purified by flash chromatography on silica gel (elution with 10% ethyl acetate in n-hexane) to provide 4-methyl-3-[(quinolin-3-yl)ethynyl]thiobenzoic acid.

후처리

  • concentrationThe reaction mixture was concentrated
  • customthe crude product was purified by flash chromatography on silica gel (elution with 10% ethyl acetate in n-hexane)
  • 출처 및 근거

    ORD 기록
    ord-4bf1055917984adcb5f73eaf99bc63a8
    출처 데이터셋
    uspto-grants-2015_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09024021B2

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