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Benzaldehyde → HCID 21529043, 화합물

HRID 1658290
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HRID 1658290 반응식
[CH:1]([N:4]([C:8]1[C:16]2[O:15][CH2:14][CH2:13][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[CH2:13][CH2:14][O:15][C:16]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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 240BenzaldehydeHCID 21529034N-(2,3-Dihydro-1-benzofuran-7-yl)-N-propan-2-ylurea

생성물 1

HCID 21529043HCID 21529043, 화합물

시약·촉매·용매 2

HCID 6395Methanesulfonic Acid촉매HCID 1140Toluene용매

실험 절차

A solution of 4.8 g. of 1-isopropyl-1-(2,3-dihydro-7-benzofuranyl)urea, 3.4 ml of benzaldehyde, 3 drops of methanesulfonic acid and 150 ml. of toluene is stirred and refluxed under a water separator for 18 hours. The cooled solution is washed with 150 ml. of 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[3,2-h]quinazolin-2(1H)-one.

후처리

  1. temperaturerefluxed under a water separator for 18 hours
  2. washThe cooled solution is washed with 150 ml
  3. dry with materialof water, dried with anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-08393d6b4a0144c699c556c26d0b13da
출처 데이터셋
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03963717

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