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Hydrogen chloride-ethyl acetate → Carbostyrilhydrochloride

HRID 39812
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반응식

HRID 39812 반응식
O1C2C=CC(CN(C3CCN(CC[N:28]4[C:37]5[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=5)[CH:31]=[CH:30][C:29]4=[O:38])CC3)C(=O)OC(C)(C)C)=CC=2OCC1.[ClH:39].C(OCC)(=O)C>>[ClH:39].[NH:28]1[C:37]2[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=2)[CH:31]=[CH:30][C:29]1=[O:38]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 21866389Hydrogen chloride-ethyl acetateHCID 59397846HCID 59397846, 화합물

생성물 1

HCID 18755291Carbostyrilhydrochloride

실험 절차

To 0.13 g of tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate, 10 mL of 4 mol/L hydrogen chloride/ethyl acetate solution was added, and left to stand at room temperature for 3 days. The solvent was removed under reduced pressure, 2-propanol was added to the residue obtained and the solvent was removed under reduced pressure. Ethyl acetate was added to the residue thus obtained and the resulting solid was filtered to afford 0.10 g of 1-(2-(4-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-quinolin-2(1H)one hydrochloride as a yellow solid.

후처리

  1. waitleft
  2. customThe solvent was removed under reduced pressure, 2-propanol
  3. additionwas added to the residue
  • customobtained
  • customthe solvent was removed under reduced pressure
  • additionEthyl acetate was added to the residue
  • customthus obtained
  • filtrationthe resulting solid was filtered
  • 출처 및 근거

    ORD 기록
    ord-a1ef0495ba5243ca90991a86a0fccf5a
    출처 데이터셋
    uspto-grants-2013_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08524738B2

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