Triethylamine → 2-(4-Methoxy-2-methylphenyl)-5-(4-pentylbicyclo[2.2.2]oct-1-yl)-1,3,4-oxadiazole

HRID 1784483

반응식

HRID 1784483 반응식
[Cl-].ClC1N(C)CC[N+]=1C.[CH3:10][C:11]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[CH:16][C:12]=1[C:13]([OH:15])=O.[CH2:22]([C:27]12[CH2:34][CH2:33][C:30]([C:35]([NH:37][NH2:38])=O)([CH2:31][CH2:32]1)[CH2:29][CH2:28]2)[CH2:23][CH2:24][CH2:25][CH3:26].C(N(CC)CC)C>C(Cl)Cl>[CH3:21][O:20][C:18]1[CH:17]=[CH:16][C:12]([C:13]2[O:15][C:35]([C:30]34[CH2:31][CH2:32][C:27]([CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])([CH2:34][CH2:33]3)[CH2:28][CH2:29]4)=[N:37][N:38]=2)=[C:11]([CH3:10])[CH:19]=1

참가 물질

6

실험 절차

2-Chloro-1,3-dimethyl-4,5-dihydro-1H-imidazol-3-ium chloride (5.07 g, 30.0 mmol) was added to a solution of 2-methyl-4-methoxybenzoic acid (2-D) (856 mg, 5.0 mmol) and 4-pentylbicyclo[2.2.2]octane-1-carbohydrazide (2-C) (1.25 g, 5.25 mmol) in methylene chloride (60 mL) followed by triethylamine (8.36 mL, 60 mmol) and the mixture stirred at room temperature for 48 h. The mixture was diluted with methylene chloride and washed with water, 1N HCl, 10% NaHCO3, brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography (silica gel, hexane:ethyl acetate, 9:1) to give 2-(4-methoxy-2-methylphenyl)-5-(4-pentylbicyclo[2.2.2]oct-1-yl)-1,3,4-oxadiazole (2-E) Mass spectrum: 369 (M+1); 1H NMR (500 MHz, CDCl3): δ 0.93 (t, 3H); 1.27 (m, 8H); 1.56 (m, 6H); 2.03 (m, 6H); 2.70 (s, 3H); 3.89 (s, 3H); 6.86 (m, 2H); 7.89 (d, 1H) ppm.

후처리

  1. washwashed with water, 1N HCl, 10% NaHCO3, brine
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated in vacuo
  4. customThe residue was purified by column chromatography (silica gel, hexane:ethyl acetate, 9:1)

출처 및 근거

ORD 기록
ord-d12e7d0d4e094acc9af766b376f160b5
출처 데이터셋
uspto-grants-2009_03
특허 번호
US07504402B2

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