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

HRID 1276608
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HRID 1276608 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 81.3%

시약·촉매·용매 1

HCID 7997Propyl Acetate용매

실험 절차

To a slurry of 2-amino-5-iodobenzoic acid (20 g, 0.076 mol) in n-propyl acetate (63 mL) was added triethylamine (11.6 mL, 0.0.84 mol) followed by n-propyl isothiocyanate (8.7 mL, 0.084 mol) at room temperature. The resulting solution was heated to reflux and the water generated was removed in a Dean Stark trap. After 4 h, the reaction mixture was cooled to room temperature and filtered. The wetcake was washed with fresh n-propyl acetate and dried at 60° C. under vacuum. In this manner, 21.4 g of the title compound was obtained as a light tan solid. See Step 1A for 1H NMR data, the UV spectrum matched that of the material made previously.

후처리

  1. temperatureThe resulting solution was heated
  2. temperatureto reflux
  3. customthe water generated was removed in a Dean Stark trap
  4. filtrationfiltered
  5. washThe wetcake was washed with fresh n-propyl acetate
  6. customdried at 60° C. under vacuum

출처 및 근거

ORD 기록
ord-0cdeababcb1543e481609e311f8aad86
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06166208

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