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HRID 923673作成日:2026年10月26日

Ethylamine → N-(4-{1,3-dimethyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl}-6-[2-(1-methylisoquinolin-6-yl)ethynyl]pyridin-2-yl)-2-(ethylamino)butanamide

https://huagongshe.com/reaction/923673

反応式

関与物質

役割名称HCID仕込み量
反応物EthylamineHCID 6341—
反応物DiisopropylethylamineHCID 81531—
反応物2-Bromobutanoyl bromideHCID 117293—
反応物4-(1,3-Dimethyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl)-6-((1-methylisoquinolin-6-yl)ethynyl)pyridin-2-amineHCID 117902868—
溶媒TolueneHCID 1140—
生成物N-(4-{1,3-dimethyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl}-6-[2-(1-methylisoquinolin-6-yl)ethynyl]pyridin-2-yl)-2-(ethylamino)butanamideHCID 117902529—

反応条件

温度0 °C

反応手順

A mixture of 4-{1,3-dimethyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl}-6-[2-(1-methylisoquinolin-6-yl)ethynyl]pyridin-2-amine (30 mg, 74 μmol), toluene (200 μl) and DIPEA (57 μl, 333 μmol) is cooled to 0° C. 2-Bromobutanoyl bromide (29 μl, 0.24 mmol) in toluene (200 μl) is added dropwise. The mixture is warmed to 50° C. and stirring is continued for 16 h. Cooled to RT 2-bromobutanoyl bromide (29 μl, 0.24 mmol) in toluene (200 μl) is added dropwise. The mixture is stirred at 60° C. for 16 h before it is again cooled to RT. Ethanamine (aqueous solution 70 wt.-%, 1 ml) is added and the mixture stirred for 16 h at 80° C. The mixture is concentrated in vacuo and the product purified by RP HPLC. Yield: 3 mg (8%). HPLC-MS: M+H=519; tR=1.37 min (METHOD—1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09278978B2
出典データセットuspto-grants-2016_03
ORD IDord-88a6499cb73e46f6a620c4d15d3506d2
出典メモuspto-grants-2016_03