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HRID 605937作成日:2026年10月26日

Diisopropylethylamine → (5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-amine

https://huagongshe.com/reaction/605937

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物4-(2-Morpholinoethoxy)anilineHCID 6484711—
反応物5,8-Dibromo-(1,2,4)triazolo(1,5-a)pyrazineHCID 49758022—
反応物4-{8-[4-(4-Methyl-piperazin-1-yl)-phenylamino]-[1,2,4]triazolo[1,5-a]pyrazin-5-yl}-thiophene-2-carboxylic acid amideHCID 57589928—
溶媒IsopropanolHCID 3776—
生成物(5-Bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-amineHCID 5759005286.2%

反応条件

温度95 °C

反応手順

According to the procedure described for Compound 6, step 1, 5,8-dibromo-[1,2,4]triazolo[1,5-a]pyrazine (0.5 g, 1.799 mmol), 4-(2-morpholin-4-yl-ethoxy)-phenylamine (0.6 g, 4.5 mmol) and N,N-diisopropylethylamine (0.47 mL, 2.7 mmol) in 2-propanol (6 mL) are stirred at 95° C. overnight. After evaporation of the solvent the residue is dissolved in DCM and washed with water (2×) and brine. The organic layer is dried over MgSO4, filtered and concentrated in vacuo to afford an oil purified by silica gel column chromatography. Elution with a 97:3 mixture DCM:MeOH gives the title compound (650 mg 86%) as a light yellow solid. LCMS: Rt 2.06 nm in (97.7%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07915256B2
出典データセットuspto-grants-2011_03
ORD IDord-6cd305aa6b7140dfb87b95a3e98f61f4
出典メモuspto-grants-2011_03