戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 968657作成日:2026年10月24日

Hydrochloric Acid → 3-(5-chloro-1-methyl-1H-indol-3-yl)-4-[1-[3-[(methylsulfonyl)oxy]propyl]-1H-indazol-3-yl]-1H-pyrrole-2,5-dione

https://huagongshe.com/ja/reaction/968657

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PyridineHCID 1049—
反応物Methanesulfonic anhydrideHCID 81560—
反応物3-(5-chloro-1-methyl-1H-indol-3-yl)-4-[1-(3-hydroxypropyl)-1H-indazol-3-yl]-1H-pyrrole-2,5-dioneHCID 10224909—
溶媒TetrahydrofuranHCID 8028—
生成物3-(5-chloro-1-methyl-1H-indol-3-yl)-4-[1-[3-[(methylsulfonyl)oxy]propyl]-1H-indazol-3-yl]-1H-pyrrole-2,5-dioneHCID 22591932—

反応条件

温度50 °C

反応手順

Pyridine (0.37 g, 4.62 mmol) and methanesulfonic anhydride (0.54 g, 3.08 mmol) were added to Compound 74 (0.67 g, 1.54 mmol) in THF (10 mL). The mixture was heated at 50° C. for 2 h, then cooled to rt. Another portion of THF (5 mL) was added, followed by 1N HCl (5 mL). The mixture was stirred for another 15 min, then extracted with EtOAc several times. The combined EtOAc layers were washed once with 1 N HCl (10 mL), water (2×20 mL) and saturated NaCl (20 mL), then dried (Na2SO4) and evaporated in vacuo to obtain 3-(5-chloro-1-methyl-1H-indol-3-yl)-4-[1-[3-[(methylsulfonyl)oxy]propyl]-1H-indazol-3-yl]-1H-pyrrole-2,5-dione as Compound 26a (0.73 g, 92%) as a reddish solid. ES-MS m/z 513 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07304060B2
出典データセットuspto-grants-2007_12
ORD IDord-27d8870f4cc24496b4ce71daf29eba5f
出典メモuspto-grants-2007_12