반응 #731155

반응 방정식

t-BuLi

5-bromo-1H-pyrazolo[3,4-c]pyridine

DMF

→

1H-pyrazolo[3,4-c]pyridine-5-carbaldehyde

수율 50.0%

용매

THF

THF

반응 조건

후처리

1. 1
   workup.ADDITIONwas added dropwise
2. 2
   기타The reaction was then carefully quenched with aq. NH4Cl
3. 3
   workup.ADDITIONdiluted with EtOAc
4. 4
   기타The resulting biphasic mixture was partitioned in a separatory funnel
5. 5
   추출The aqueous portion was extracted three tines with EtOAc
6. 6
   세척the combined organic extracts were washed with brine
7. 7
   건조dried over MgSO4
8. 8
   여과Filtration and concentration under reduced pressure

실험 절차

t-BuLi (27 mL, 1.7 M in pentane) was added to 100 mL of THF at −78° C. 5-bromo-1H-pyrazolo[3,4-c]pyridine (3.0 g, 15 mmol) was added dropwise to the solution in 50 ml of THF via addition funnel. The resulting mixture was stirred for 1 h, at which point DMF (6.0 mL, 76 mmol) was added dropwise. The reaction mixture was allowed to warm to room temperature and stirred 2 h. The reaction was then carefully quenched with aq. NH4Cl and diluted with EtOAc. The resulting biphasic mixture was partitioned in a separatory funnel. The aqueous portion was extracted three tines with EtOAc, and the combined organic extracts were washed with brine and dried over MgSO4. Filtration and concentration under reduced pressure, followed by flash chromatography on silica gel (100% CH2Cl2 to 7.5% MeOH/CH2Cl2), afforded the desired 1H-pyrazolo[3,4-c]pyridine-5-carbaldehyde (1.1 g, 50% yield) as a white solid. H1 NMR (MeOD, 400 MHz) keto tautomer: 10.17 (s, 1H), 9.19 (s, 1H), 8.56 (s, 1H), 8.46 (s, 1H); enol tautomer: 9.00 (s, 1H), 8.25 (s, 1H), 8.05 (s, 2H), 5.73 (s, 1H). MS (API-ES) m/z (%): 147 (100%, M++1).

출처