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HRID 348962作成日:2026年10月26日

Butyl iodide → 1-Butyl-4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylic acid

https://huagongshe.com/reaction/348962

反応式

関与物質

役割名称HCID仕込み量
反応物Butyl iodideHCID 10962—
反応物Potassium HydroxideHCID 14797—
反応物methyl 4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylateHCID 21086207—
溶媒DimethylformamideHCID 6228—
生成物1-Butyl-4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylic acidHCID 21085174—

反応条件

温度70 °C

反応手順

To a mixture of methyl 4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylate (0.437 g) in DMF(15 mL) was added potassium hydroxide (0.087 g) and iodobutane (0.34 mL). The mixture was heated to 70° C. for 6 h. then stirred at room temperature for 72 h. The mixture was partitioned between water and ethyl acetate, the layers were separated and the organic layer washed three times with water. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated. The residue was dissolved in methanol (5 mL) to which was added 1N NaOH (2 mL) and the mixture heated to 50° C. for 1 h. The mixture was cooled to room temperature and poured into water and washed with ether. The aqueous layer was acidified to pH 4 with 1N HCl and the product extracted into ethyl acetate which was dried over anhydrous sodium sulfate, filtered and concentrated to dryness to give 0.377 g of the title compound: 1H NMR (CDCl3) δ 0.973, 1.38, 1.87, 3.01, 3.45, 4.21, 6.71, 7.36, 7.82, 8.18.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07176242B2
出典データセットuspto-grants-2007_02
ORD IDord-385f4bb1a3254dd98da25b54207bc336
出典メモuspto-grants-2007_02