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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1171123생성일: 2026년 10월 27일

Acetic Acid → HCID 178489372, 화합물

https://huagongshe.com/reaction/1171123

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물5-bromo-3-(2-methoxy-phenyl)-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-b]pyridineHCID 59836032—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물HCID 178489372HCID 17848937297%

반응 조건

온도70 °C

반응 단계

To a solution of 5-bromo-3-(2-methoxy-phenyl)-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-b]pyridine (260 mg, 0.60 mmol) in THF (3 mL) was added tetrabutylammonium fluoride (6 mL of 1 M in THF solution, 6.00 mmol) and molecular sieves. The solution was heated under reflux (70° C.) for 4 hours without stirring. The solution was cooled to ambient temperature and acidified to pH=5 by adding dropwise a dilute solution of acetic acid in MeOH. The solution was filtered and the filtrate was concentrated via rotary evaporation. The material was extracted into EtOAc and washed 3×H2O. The organic layer was dried over Na2SO4 and concentrated down to afford 5-bromo-3-(2-methoxy-phenyl)-1H-pyrazolo[3,4-b]pyridine as an orange solid (177 mg, 97% yield). MS: m/z 303.9, 305.9 [M+H+]. The material was used directly in step 2 without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07829558B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-c59327663e77453189bd64494105215f
출처 메모uspto-grants-2010_11