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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 662016생성일: 2026년 10월 24일

Sodium Azide → 5-(Azidomethyl)-1,6-diethyl-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridin-4-amine

https://huagongshe.com/ko/reaction/662016

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참여 물질

역할이름HCID투입량
반응물Sodium AzideHCID 33557—
반응물[1,6-Diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methanolHCID 59683222—
촉매Thionyl ChlorideHCID 24386—
용매Dimethyl SulfoxideHCID 679—
생성물5-(Azidomethyl)-1,6-diethyl-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridin-4-amineHCID 59683232218.1%

반응 조건

온도80 °C

반응 단계

To [1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methanol (24.9 g, 82 mmol) was added thionyl chloride (90 mL, 1.23 mmol) and the mixture was heated to 80° C. under an atmosphere of nitrogen. After 2 h the mixture was cooled, evaporated and the residue azeotroped with toluene. The residue was then dissolved in a solution of sodium azide (7.98 g, 123 mmol) in DMSO (120 mL). The mixture was stirred for 16 h. The above procedure was repeated on the same scale and the 2 reactions combined for work-up. The combined DMSO mixture was partitioned between ethyl acetate and aqueous sodium bicarbonate. The aqueous phase was extracted thoroughly with ethyl acetate and the combined organics were washed with water, then brine, dried and evaporated to afford 58.9 g of a brown solid. The product was purified by flash chomatography on 1.5 kg of silica using a step gradient from 3:1 to 2:1 cyclohexane/ethyl acetate to afford 39.94 g of the title compound. LC-MS m/z 330 (M+H)+, 2.21 min (ret time).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08084449B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-b3c3c1f8012940c6aa74fd9fb268e2df
출처 메모uspto-grants-2011_12