Sodium hydride → 3,8-Dimethyl-1-oxo-2-phenyl-1,2-dihydro-isoquinoline-4-carboxylic acid ethyl ester

HRID 1920736

반응식

HRID 1920736 반응식
Br[C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:3]=1[C:4](O)=[O:5].[CH2:12]([O:14][C:15](=[O:26])[CH:16]=[C:17]([NH:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH3:18])[CH3:13].[H-].[Na+]>C(#N)C>[CH2:12]([O:14][C:15]([C:16]1[C:2]2[C:3](=[C:7]([CH3:11])[CH:8]=[CH:9][CH:10]=2)[C:4](=[O:5])[N:19]([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[C:17]=1[CH3:18])=[O:26])[CH3:13]

참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 94928Ethyl 3-anilinobut-2-enoateHCID 27355892-Bromo-6-methylbenzoic acid

생성물 1

HCID 577333143,8-Dimethyl-1-oxo-2-phenyl-1,2-dihydro-isoquinoline-4-carboxylic acid ethyl ester수율 22.3%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a cold (ice/water bath) solution of 2-bromo-6-methyl-benzoic acid (650 mg, 3.023 mmol) and 3-phenylamino-but-2-enoic acid ethyl ester (750 mg, 3.65 mmol) in acetonitrile (10 ml), sodium hydride (267 mg, 6.67 mmol, 60% dispersion in mineral oil) was added in portions. The cold bath was removed and the mixture was sonicated at ambient temperature until gas evolution ceased (10 min). Copper (I) bromide was added (957 mg, 6.67 mmol) and the obtained suspension was flushed with argon, sealed and heated under microwave irradiation at +80° C. for 30 min. LC-MS indicated a full conversion to 2-(1-ethoxycarbonyl-2-phenylamino-propenyl)-6-methyl-benzoic acid (LC-MS (m/z) 340.4 (MH+); tR=1.59. The obtained suspension was heated at +160° C. under microwave irradiation for 30 min. It was diluted with ethyl acetate (50 ml) and filtered. The obtained organic solution was washed with 1M HCl (3×50 ml), water (2×10 ml) and sat. aq. NaHCO3 solution (30 ml), absorbed on SiO2 (3 g) and flash chromatographed on SiO2 (50 g, gradient heptane-30% ethyl acetate in heptane) to give 217 mg of yellow oil. Yield 22%. LC-MS (m/z) 322.2 (MH+); tR=1.62. 1H NMR (500 MHz, DMSO-d6): 1.32 (t, 3H), 1.91 (s, 3H), 2.74 (s, 3H), 4.39 (q, 2H), 7.3 (d, 1H), 7.36 (overlapping m, 3H), 7.49 (m, 1H), 7.55 (t, 2H), 7.61 (t, 1H).

후처리

  1. customThe cold bath was removed
  2. customthe mixture was sonicated at ambient temperature until gas evolution
  3. custom(10 min)
  4. additionCopper (I) bromide was added (957 mg, 6.67 mmol)
  5. customthe obtained suspension was flushed with argon
  6. customsealed
  7. temperatureheated under microwave irradiation at +80° C. for 30 min
  8. temperatureThe obtained suspension was heated at +160° C. under microwave irradiation for 30 min
  9. additionIt was diluted with ethyl acetate (50 ml)
  10. filtrationfiltered
  11. washThe obtained organic solution was washed with 1M HCl (3×50 ml), water (2×10 ml) and sat. aq. NaHCO3 solution (30 ml)
  12. customabsorbed on SiO2 (3 g) and flash
  13. customchromatographed on SiO2 (50 g, gradient heptane-30% ethyl acetate in heptane)

출처 및 근거

ORD 기록
ord-5a611331ae3441ccac94e9a592e271fd
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08173639B2

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