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Acetohydrazide → 7-Bromo-9-chloro-1-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline

HRID 1521625
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HRID 1521625 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([Cl:12])[CH:11]=1)[NH:8][C:7](=S)[CH2:6][CH2:5]2.[C:14]([NH:17][NH2:18])(=O)[CH3:15]>C1(O)CCCCC1>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([Cl:12])[CH:11]=1)[N:8]1[C:14]([CH3:15])=[N:17][N:18]=[C:7]1[CH2:6][CH2:5]2
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참가 물질

4

반응물 2

HCID 14039AcetohydrazideHCID 899616046-bromo-8-chloro-3,4-dihydroquinoline-2(1H)-thione

생성물 1

HCID 709778617-Bromo-9-chloro-1-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline

시약·촉매·용매 1

HCID 7966Cyclohexanol용매

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온도
100 °C

실험 절차

To a solution of 6-bromo-8-chloro-3,4-dihydroquinoline-2(1H)-thione (80-2; 0.45 g, 0.0016 mol) in cyclohexanol (20 mL) was added acetic hydrazide (0.241 g, 0.0032 mol) and the reaction mixture was heated at 100° C. for 1 h under microwave irradiation conditions. Then 1.5 g of molecular sieves powder was added and the reaction mixture was again heated at 190° C. for 2 h under microwave conditions. The reaction mixture was filtered and the filtrate was evaporated. The crude was purified by silica gel column chromatography to obtain title compound. 1H NMR (400 MHz, DMSO-d6) δ: 7.85 (s, 1H), 7.76 (s, 1H), 2.87 (bs, 4H), 2.50 (s, 3H). MS (M+1): 298.2.

후처리

  1. additionThen 1.5 g of molecular sieves powder was added
  2. temperaturethe reaction mixture was again heated at 190° C. for 2 h under microwave conditions
  3. filtrationThe reaction mixture was filtered
  4. customthe filtrate was evaporated
  5. customThe crude was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-807bcec6dab040f4af4d0eed16432e81
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073929B2

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