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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 536529생성일: 2026년 10월 27일

Diisopropylethylamine → 2-[5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-4-(3-hydroxyazetidin-1-yl)-5,5-dimethyl-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one

https://huagongshe.com/reaction/536529

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물3-Hydroxyazetidine hydrochlorideHCID 2759290—
반응물Trifluoroacetic acid waterHCID 22392675—
반응물2-[5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-4-iodo-5,5-dimethyl-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-oneHCID 86705366—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2-[5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-4-(3-hydroxyazetidin-1-yl)-5,5-dimethyl-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-oneHCID 7128583922.1%

반응 조건

온도150 °C

반응 단계

100 mg (0.18 mmol, approx. 95% purity) of 2-[5-fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-4-iodo-5,5-dimethyl-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one (example 16A) was dissolved in 1-methyl-2-pyrrolidone (3.1 ml) in a reaction vessel suitable for a microwave, and 0.19 ml (1.07 mmol) of N,N-diisopropyl ethylamine and 97 mg (0.89 mmol) of azetidin-3-ol hydrochloride were added. Then the reaction vessel was sealed with a septum and was heated in the microwave at 150° C. for 3 h. After cooling, water/trifluoroacetic acid was added to the reaction mixture and the resultant solid was filtered off. The filtrate was purified by preparative HPLC (acetonitrile:water (+0.1% trifluoroacetic acid) gradient). 19 mg of the title compound was obtained (21% of theor.; purity 93%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859569B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-b44c7845157448c99d00d3338f6f499a
출처 메모uspto-grants-2014_10