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Benzaldehyde → 1-isopropyl-3,4,7,8-tetrahydro-4-phenyl-furo[2,3-h]quinazolin-2(1H)-one

HRID 1658281
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HRID 1658281 반응식
[CH:1]([N:4]([C:8]1[C:13]2[CH2:14][CH2:15][O:16][C:12]=2[CH:11]=[CH:10][CH:9]=1)[C:5]([NH2:7])=[O:6])([CH3:3])[CH3:2].[CH:17](=O)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>CS(O)(=O)=O.C1(C)C=CC=CC=1>[CH:1]([N:4]1[C:8]2[C:9](=[CH:10][CH:11]=[C:12]3[O:16][CH2:15][CH2:14][C:13]3=2)[CH:17]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[NH:7][C:5]1=[O:6])([CH3:3])[CH3:2]
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참가 물질

5

반응물 2

HCID 240BenzaldehydeHCID 21529030N-(2,3-Dihydro-1-benzofuran-4-yl)-N-propan-2-ylurea

생성물 1

HCID 681363431-isopropyl-3,4,7,8-tetrahydro-4-phenyl-furo[2,3-h]quinazolin-2(1H)-one

시약·촉매·용매 2

HCID 6395Methanesulfonic Acid촉매HCID 1140Toluene용매

실험 절차

A solution of 5.0 g. of 1-isopropyl-1-(2,3-dihydro-4-benzofuranyl)urea, 3.5 ml. of benzaldehyde, 3 drops of methanesulfonic acid and 150 ml. of toluene is stirred and refluxed under a water separator for 20 hours. The resulting solution is cooled and the cooled solution is washed with 150 ml. water, dried with anhydrous magnesium sulfate, filtered and concentrated in vacuo to give an oil of 1-isopropyl-3,4,7,8-tetrahydro-4-phenyl-furo[2,3-h]quinazolin-2(1H)-one.

후처리

  1. temperaturerefluxed under a water separator for 20 hours
  2. temperatureThe resulting solution is cooled
  3. washthe cooled solution is washed with 150 ml
  4. dry with materialwater, dried with anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-2f8a7e0db479476aba043977f594bd89
출처 데이터셋
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03963717

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