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HRID 14180作成日:2026年10月26日

Methyl 1-butyl-4-iodo-1H-indole-6-carboxylate → Methyl 1-butyl-4-cyano-1H-indole-6-carboxylate

https://huagongshe.com/reaction/14180

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 1-butyl-4-iodo-1H-indole-6-carboxylateHCID 21086136—
反応物HCID 178418546HCID 178418546—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物Methyl 1-butyl-4-cyano-1H-indole-6-carboxylateHCID 2108613547.4%

反応条件

温度150 °C

反応手順

To a mixture of methyl 1-butyl-4-iodo-1H-indole-6-carboxylate (Example SP-218, Step 4) (1.47 g) in N-methyl pyrrolidinone (15 mL) was added copper (I) cyanide (1.1 g). The mixture was heated to 150° C. for 6 h, removed from heat and cooled to room temperature. The mixture was partitioned between water and ethyl acetate and the layers were separated. The organic layer was washed three times with water, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Column chromatography on silica gel (100 mL) using 20% ethyl acetate as eluent to give 0.5 g of the title compound: 1H NMR (CDCl3) δ 0.955, 1.32, 1.85, 3.98, 4.23, 6.76, 7.43, 8.16, 8.30.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727997B2
出典データセットuspto-grants-2010_06
ORD IDord-508a6e30e6544766b9749c4d8ed0c4c4
出典メモuspto-grants-2010_06