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HCID 12939743, 화합물 → HCID 12939745, 화합물

HRID 847767
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반응식

HRID 847767 반응식
[NH:1]1[C:9]2[C:4](=[N:5][CH:6]=[CH:7][CH:8]=2)[N:3]=[C:2]1[S:10][CH:11]([C:16](=O)[C:17]1[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][CH:18]=1)[CH2:12][C:13]([OH:15])=[O:14]>FC(F)(F)C(O)=O>[Cl:23][C:20]1[CH:21]=[CH:22][C:17]([C:16]2[N:1]3[C:9]4[C:4]([N:3]=[C:2]3[S:10][C:11]=2[CH2:12][C:13]([OH:15])=[O:14])=[N:5][CH:6]=[CH:7][CH:8]=4)=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 12939743HCID 12939743, 화합물

생성물 1

HCID 12939745HCID 12939745, 화합물수율 57.6%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

17 g (0.047 m) of 3-(imidazo[4,5-b]pyridine-2-ylthio)-3-(4-chlorobenzoyl)propionic acid, prepared according to Example 2, is dissolved in 200 ml trifluoroacetic acid, and the solution is heated to gentle reflux overnight. The solution is cooled and filtered, the solvent is removed in vacuo and the residual solid triturated with ether and the solid collected. The resulting trifluoroacetate is disproportionated in hot acetonitrile to give 9.3 g of title compound, m.p. 250°-252° C.

후처리

  1. temperaturethe solution is heated
  2. temperatureto gentle reflux overnight
temperature
The solution is cooled
  • filtrationfiltered
  • customthe solvent is removed in vacuo
  • customthe residual solid triturated with ether
  • customthe solid collected
  • 출처 및 근거

    ORD 기록
    ord-ed3f2308d1124396a094389c0bef8e52
    출처 데이터셋
    uspto-grants-1981_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04293696

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