Potassium Carbonate → 5-tert-Butyl-2-{1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1H-imidazol-4-yl}-2H-pyrazol-3-ylamine
반응식
[C:1]([C:5]1[CH:6]=[C:7]([NH2:10])[NH:8][N:9]=1)([CH3:4])([CH3:3])[CH3:2].C([O-])([O-])=O.[K+].[K+].CN[C@@H]1CCCC[C@H]1NC.I[C:28]1[N:32]([CH2:33][CH2:34][O:35][CH:36]2[CH2:41][CH2:40][CH2:39][CH2:38][O:37]2)[CH:31]=[N:30][CH:29]=1>[Cu]I.O.C1(C)C=CC=CC=1>[C:1]([C:5]1[CH:6]=[C:7]([NH2:10])[N:8]([C:29]2[N:30]=[CH:31][N:32]([CH2:33][CH2:34][O:35][CH:36]3[CH2:41][CH2:40][CH2:39][CH2:38][O:37]3)[CH:28]=2)[N:9]=1)([CH3:4])([CH3:3])[CH3:2]참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 150 °C
실험 절차
To a mixture of Intermediate 119a (1.50 g, 4.66 mmol), 5-tert-butyl-2H-pyrazol-3-ylamine (648 mg, 4.66 mmol), copper(I)iodide (44 mg, 0.23 mmol) and K2CO3 (1.35 g, 9.78 mmol) was added a solution of toluene (10 mL), previously degassed by using a stream of argon. (R,R)-(−)-N,N′-Dimethyl-1,2-cyclohexanediamine (147 μL, 0.93 mmol) was then added and the reaction mixture was heated at 150° C. for 3 h under microwave irradiation. The crude reaction mixture was poured into water and extracted with EtOAc (×3). The combined organic layers were washed with brine, dried (MgSO4) and concentrated in vacuo. The resultant residue was purified by FCC on silica, using a gradient of 0-100% EtOAc in cyclohexane, to give a product consisting of the title compound (550 mg) in mixture with the un-reacted 5-iodo-1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1H-imidazole isomer. LCMS (Method 4): Rt 2.32 min, m/z 334 [MH+].
후처리
- custompreviously degassed
- customThe crude reaction mixture
- extractionextracted with EtOAc (×3)
- washThe combined organic layers were washed with brine
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customThe resultant residue was purified by FCC on silica
- customto give a product
출처 및 근거
- ORD 기록
- ord-1f86f72861c54058b54550f69b7c658d
- 출처 데이터셋
- uspto-grants-2015_09
- 특허 번호
- US09139584B2
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