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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 510115생성일: 2026년 10월 27일

Isopropanol → 2-[1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-6-isopropoxy-7-methyl-7,9-dihydro-8H-purin-8-one

https://huagongshe.com/reaction/510115

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참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물Cesium carbonateHCID 10796—
반응물3,4,7,8-Tetramethyl-1,10-phenanthrolineHCID 74265—
반응물2-[1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-6-iodo-7-methyl-7,9-dihydro-8H-purin-8-oneHCID 86720052—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2-[1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-6-isopropoxy-7-methyl-7,9-dihydro-8H-purin-8-oneHCID 66614319—

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온도140 °C

반응 단계

200 mg (0.399 mmol) of the compound obtained in example 107 were admixed in a microwavable flask with isopropanol (3 ml), 260 mg (0.798 mmol) of cesium carbonate, 8 mg (0.04 mmol) of copper(I) iodide and 19 mg (0.08 mmol) of 3,4,7,8-tetramethyl-1,10-phenanthroline. The flask was purged with argon while being treated with ultrasound for 5 min, and then closed with an appropriate septum. Then it was heated in a microwave at 140° C. for 2 h. Reaction monitoring showed low conversion. For that reason, N-methylpyrrolidone (1 ml) was added and the mixture was once again heated in a microwave at 140° C. for 2 h and then at 180° C. for 8 h. After cooling, the reaction mixture was filtered and concentrated, and the residue was purified by means of preparative HPLC (acetonitrile:water (+0.05% formic acid) gradient). 21 mg of the title compound were obtained (12% of theory).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096592B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-93e140ad3a6242eda03f4f74f49d346d
출처 메모uspto-grants-2015_08