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HRID 536507作成日:2026年10月25日

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

https://huagongshe.com/reaction/536507

反応式

関与物質

役割名称HCID仕込み量
反応物4,4,4-TrifluorobutylamineHCID 136645—
反応物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-oneHCID 86705366—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物2-[5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-5,5-dimethyl-4-[(4,4,4-trifluorobutyl)amino]-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-oneHCID 71285652—

反応条件

温度150 °C

反応手順

150 mg (0.186 mmol, approx. 66% purity) of the compound obtained in example 16A was dissolved in 1-methyl-2-pyrrolidone (3 ml) in a reaction vessel suitable for a microwave and 0.4 ml of 4,4,4-trifluorobutylamine was added. Then it was sealed with a corresponding septum and it was heated in the microwave at 150° C. for 3 h. After cooling, the reaction mixture was purified by preparative HPLC (acetonitrile:water (+0.05% formic acid) gradient). 47 mg of the title compound was obtained (48% of theor.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08859569B2
出典データセットuspto-grants-2014_10
ORD IDord-2e264ea1807446199134889ce89898ed
出典メモuspto-grants-2014_10