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HRID 1733856作成日:2026年10月25日

5-Methoxy-2-methylindole → 4-(2-(5-Methoxy-2-methyl-1H-indol-3-YL)ethyl)morpholine

https://huagongshe.com/reaction/1733856

反応式

関与物質

役割名称HCID仕込み量
反応物5-Methoxy-2-methylindoleHCID 70642—
反応物4-(2-iodoethyl)morpholineHCID 11149168—
反応物HCID 178418689HCID 178418689—
触媒ZincchlorideHCID 3007855—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium BicarbonateHCID 516892—
生成物4-(2-(5-Methoxy-2-methyl-1H-indol-3-YL)ethyl)morpholineHCID 194388097%

反応手順

To 5-methoxy-2-methyl-1H-indole (5.00 g; 31.0 mmol) in 30 mL of dry THF at 0° C. was added dropwise MeMgBr (3.0M in Et2O; 11.4 mL; 34.2 mmol). The solution was stirred 30 min at r.t. after which ZnCl2 (0.5M in THF; 64 mL; 32 mmol) was added. The mixture was stirred at r.t., after 1 h, N-(2-iodoethyl)morpholine (14.41 g; 51.5 mmol) was added. The final mixture was stirred at r.t. overnight. The mixture was poored in saturated NaHCO3 (100 mL), extracted with EtOAc (2×100 mL). The organic phase was washed with brine (100 mL), dried over Na2SO4, filtered, concentrated and flash chromatographed (Silica gel; EtOAc/Ace O to 10%) to yield 587 mg (7%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05532237
出典データセットuspto-grants-1996_07
ORD IDord-6331567eb402415e913afdc0262b9613
出典メモuspto-grants-1996_07