Triethylamine → HCID 11508173, 화합물

HRID 735241노트

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HRID 735241 반응식
[Cl:1][C:2]1[CH:11]=[C:10](Cl)[CH:9]=[C:8]2[C:3]=1[C:4](=[O:21])[C:5]([CH3:20])([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:6](=[O:13])[NH:7]2.C([O-])([O-])=O.[K+].[K+].[CH2:28]([N:30](CC)[CH2:31]C)C.Cl.CNC>CC#N>[Cl:1][C:2]1[CH:11]=[C:10]([N:30]([CH3:31])[CH3:28])[CH:9]=[C:8]2[C:3]=1[C:4](=[O:21])[C:5]([CH3:20])([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:6](=[O:13])[NH:7]2

참가 물질

6

실험 절차

To a solution of 5,7-dichloro-3-methyl-3-phenyl-1H-quinoline-2,4-dione (1.00 g, 3.12 mmol) in MeCN (10 mL) were added K2CO3 (0.65 g, 4.68 mmol), triethylamine (0.65 mL, 4.68 mmol), and dimethylamine hydrochloride (0.35 g, 7.80 mmol) at room temperature. The reaction mixture was then heated for 10 hours at reflux temperature. After the reaction completed, the solvent was removed. The residue was diluted with 1N HCl solution and extracted with ethyl acetate (100 mL×2). The organic phase was dried over magnesium sulfate and concentrated in vacuo. The crude was purified by a column chromatography on silica gel to give the objective compound (0.67 g, 65%): 1H NMR (200 MHz, CDCl3) δ 1.89 (s, 3H, CH3), 2.64 (s, 6H, 2NCH3), 6.29 (d, J=2.03 Hz, 1H, ArH), 6.49 (d, J=2.03 Hz, 1H, ArH), 7.23-7.33 (m, 5H, ArH), 9.13 (br s, 1H, NH); m.p. 224-226° C.; MS(EI) m/e 328 [M+], 313, 196, 132; HRMS m/e cacld. for C18H17N2O2Cl 328.0979, found 328.0979.

후처리

  1. temperatureThe reaction mixture was then heated for 10 hours
  2. temperatureat reflux temperature
  3. customthe solvent was removed
  4. additionThe residue was diluted with 1N HCl solution
  5. extractionextracted with ethyl acetate (100 mL×2)
  6. dry with materialThe organic phase was dried over magnesium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe crude was purified by a column chromatography on silica gel

출처 및 근거

ORD 기록
ord-b3ed995d4991413093fdde097db76e32
출처 데이터셋
uspto-grants-2009_09
특허 번호
US07592457B2

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