반응식
I[C:2]1[CH:10]=[N:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].C(=O)([O-])[O-].[K+].[K+].[F:17][C:18]1[CH:19]=[CH:20][C:21]([CH3:37])=[C:22]([N:24]2[C:28]([NH2:29])=[C:27]([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)[C:26]([CH3:36])=[N:25]2)[CH:23]=1.C1(C(C(C)=O)C#N)C=CC=CC=1>CN(C=O)C.C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[F:17][C:18]1[CH:19]=[CH:20][C:21]([CH3:37])=[C:22]([N:24]2[C:28]([NH:29][C:2]3[CH:10]=[N:9][CH:8]=[CH:7][C:3]=3[C:4]([OH:6])=[O:5])=[C:27]([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)[C:26]([CH3:36])=[N:25]2)[CH:23]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 150 °C
실험 절차
A mixture of 3-iodoisonicotinic acid (180 mg, 0.72 mmol), potassium carbonate (199 mg, 1.44 mmol), 1-(5-fluoro-2-methylphenyl)-3-methyl-4-phenyl-1H-pyrazol-5-amine (202 mg, 0.72 mmol, synthesized in the same manner as Intermediate F, using commercially available 2-phenylacetoacetonitrile as the nitrile source), and copper (II) acetate (6.5 mg, 0.04 mmol) in DMF (1 mL) was heated (150° C.) in a sealed tube for 16 h. The mixture was cooled to rt, filtered through a silica gel plug using ethyl acetate as eluent, concentrated to dryness, and subjected to HPLC purification using a gradient elution from 30% to 90% acetonitrile in water to afford 29.1 mg (10%) of the desired product. 1H NMR (300 MHz, CD3CN) δ 9.39 (br s, 1H), 7.93 (s, 1H), 7.86-7.90 (m, 2H), 7.05-7.45 (m, 8H), 2.38 (s, 3H), 2.15 (s, 3H); ES-MS m/z 403.1 (MH+), HPLC RT (min) 2.40.
후처리
- customsynthesized in the same manner as Intermediate F
- temperatureThe mixture was cooled to rt
- filtrationfiltered through a silica gel plug
- concentrationconcentrated to dryness
- customsubjected to HPLC purification
- washa gradient elution from 30% to 90% acetonitrile in water
출처 및 근거
- ORD 기록
- ord-f310d383af404a42a984fc774f7260d8
- 출처 데이터셋
- uspto-grants-2009_04
- 특허 번호
- US07517878B2
연결된 노트
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