Trifluoroacetic acid → ethyl 6-cyclopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylate
반응식
[CH:1]1([C:4]2[CH:5]=[C:6]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[C:7]3[CH:12]=[N:11][N:10](CC4C=CC(OC)=CC=4)[C:8]=3[N:9]=2)[CH2:3][CH2:2]1.FC(F)(F)C(O)=O.C1(OC)C=CC=CC=1>>[CH:1]1([C:4]2[CH:5]=[C:6]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[C:7]3[CH:12]=[N:11][NH:10][C:8]=3[N:9]=2)[CH2:2][CH2:3]1참가 물질
실험 절차
To a 20 mL microwave vial were combined ethyl 6-cyclopropyl-1-{[4-(methyloxy)phenyl]methyl}-1H-pyrazolo[3,4-b]pyridine-4-carboxylate (2.05 g, 5.83 mmol), trifluoroacetic acid (6.74 ml, 88 mmol) and anisole (1.912 ml, 17.50 mmol). The reaction vessel was sealed and irradiated (microwave) at 100° C. for 5 minutes. After cooling to room temperature, the reaction mixture was concentrated in vacuo. The residue was diluted with water (20 mL) and then saturated NaHCO3 until basic. The contents were extracted with DCM (4×20 mL). The combined organic layers were washed with water, brine, dried over MgSO4, filtered and concentrated in vacuo. The crude product was purified via silica gel chromatography (eluent: 0 to 20% EtOAc:Hex). The final product was obtained as 1.06 g (79%). LCMS E-S (M+H)=232.2. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.95-1.21 (m, 4H) 1.41 (t, J=7.07 Hz, 3H) 2.33-2.46 (m, 1H) 4.44 (q, J=7.07 Hz, 2H) 7.67 (s, 1H) 8.26 (d, J=1.26 Hz, 1H) 13.75 (s, 1H).
후처리
- customThe reaction vessel was sealed
- customirradiated (microwave) at 100° C. for 5 minutes
- concentrationthe reaction mixture was concentrated in vacuo
- additionThe residue was diluted with water (20 mL)
- extractionThe contents were extracted with DCM (4×20 mL)
- washThe combined organic layers were washed with water, brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe crude product was purified via silica gel chromatography (eluent: 0 to 20% EtOAc:Hex)
출처 및 근거
- ORD 기록
- ord-ce36bd7875244a688b3ce6bb3e9fad16
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08637509B2
반응 노트
불러오는 중…