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Triethylamine → 2,3-Dihydro-6-iodo-3-propyl-2-thioxo-4(1H)-quinazolinone

HRID 1276607
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HRID 1276607 반응식
[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([I:11])=[CH:7][C:3]=1[C:4]([OH:6])=O.C(N(CC)CC)C.[CH2:19]([N:22]=[C:23]=[S:24])[CH2:20][CH3:21]>C(OCCC)(=O)C>[I:11][C:8]1[CH:7]=[C:3]2[C:2](=[CH:10][CH:9]=1)[NH:1][C:23](=[S:24])[N:22]([CH2:19][CH2:20][CH3:21])[C:4]2=[O:6]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 69403Propyl IsothiocyanateHCID 72911Benzoic acid, 2-amino-5-iodo-

생성물 1

HCID 108933552,3-Dihydro-6-iodo-3-propyl-2-thioxo-4(1H)-quinazolinone수율 85.9%

시약·촉매·용매 1

HCID 7997Propyl Acetate용매

실험 절차

To a slurry of 2-amino-5-iodobenzoic acid (100 g, 0.38 mol) in n-propyl acetate (315 mL) was added triethylamine (58 mL, 0.42 mol) at room temperature. The resulting solution was heated to reflux and n-propyl isothiocyanate (43 mL, 0.42 mol) was added over a one hour period. The reaction mixture was maintained at reflux for 18 h, then cooled to room temperature and filtered. The wetcake was washed with fresh propyl acetate and dried at 60° C. under vacuum. In this manner, 113 g of the title compound was obtained as a tan solid. m.p.>200° C.; 1H NMR (Me2SO--d6): δ13.02 (bs,1H), 8.22 (d,1H), 8.06 (dd,1H), 7.21 (d,1H), 4.34 (m,2H), 1.69 (m,2H), 0.93 (t,3H).

후처리

  1. temperatureThe resulting solution was heated
  2. temperatureto reflux
  3. temperatureThe reaction mixture was maintained
  4. temperatureat reflux for 18 h
  5. filtrationfiltered
  6. washThe wetcake was washed with fresh propyl acetate
  7. customdried at 60° C. under vacuum

출처 및 근거

ORD 기록
ord-7fa1ff2483104a9584c08f248a340520
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06166208

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