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HRID 7482作成日:2026年10月23日

Hydrochloric Acid → 4-Chloro-6-methoxy-7-(3-morpholinopropoxy)cinnoline

https://huagongshe.com/ja/reaction/7482

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物4-(3-Chloropropyl)morpholineHCID 95834—
反応物4-Chloro-7-hydroxy-6-methoxycinnolineHCID 135752523—
溶媒IsopropanolHCID 3776—
溶媒DimethylformamideHCID 6228—
溶媒Methanol--water (1/1)HCID 22242641—
生成物4-Chloro-6-methoxy-7-(3-morpholinopropoxy)cinnolineHCID 21991059—

反応条件

温度80 °C

反応手順

The starting material 4-chloro-6-methoxy-7-(3-morpholinopropoxy)cinnoline hydrochloride was obtained by adding 1-chloro-3-morpholinopropane (190 mg, 0.95 mmol), (prepared as described in U.S. Pat. No. 4,004,007), to a suspension of 4-chloro-7-hydroxy-6-methoxycinnoline (0.2 g, 0.95 mmol), (prepared as described for the starting material in Example 10), in DMF (5 ml) containing potassium carbonate (327 mg, 2.3 mmol) and potassium iodide (15 mg, 0.095 mmol). After heating at 80° C. for 2 hours, potassium carbonate (65 mg, 0.47 mmol) and more 1-chloro-3-morpholinopropane (95 mg, 0.47 mmol) were added. After stirring for 4 hours at 80° C. the reaction mixture was cooled and 7M hydrogen chloride in isopropanol (407 μl) was added. The solution was poured onto a Diaion (trade mark of Mitsubishi) HP20SS column, using water/methanol (100/0 to 0/100 as a gradient) to give 4-chloro-6-methoxy-7-(3-morpholinopropoxy)cinnoline as an hydrochloride salt (175 mg, 44%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087602B2
出典データセットuspto-grants-2006_08
ORD IDord-245f2870f5024f29a93ebbc4e31b8a82
出典メモuspto-grants-2006_08