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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 564432생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/564432

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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, concentrated 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 concentrated to afford 58.9 g of a brown solid. The product was purified by flash chromatography 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 번호US08067408B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-cb14ebfd6ab0473faa3a31bd4f339675
출처 메모uspto-grants-2011_11