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HRID 22999作成日:2026年10月26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/reaction/22999

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 1N 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US06849643B2
出典データセットuspto-grants-2005_02
ORD IDord-560ee865923648af9f817541c30ea563
出典メモuspto-grants-2005_02