戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 24040作成日:2026年10月24日

Methyl propiolate → 3-{5-[2-(2-Methyl-[1,8]naphthyridin-3-yl)-ethyl]-indol-1-yl}-acrylic acid methyl ester

https://huagongshe.com/ja/reaction/24040

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl propiolateHCID 13536—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物2-methyl-3-[2-(1-triisopropylsilanyl-1H-indol-5-yl)-ethyl]-[1,8]naphthyridineHCID 22570268—
生成物3-{5-[2-(2-Methyl-[1,8]naphthyridin-3-yl)-ethyl]-indol-1-yl}-acrylic acid methyl esterHCID 6682136966%

反応手順

A mixture of 2-methyl-3-[2-(1-triisopropylsilanyl-1H-indol-5-yl)-ethyl]-[1,8]naphthyridine (0.25 g, 0.74 mmol), propynoic acid methyl ester (0.07 g, 0.84 mmol), and tetrabutylammonium fluoride [1.0 M] (2.23 mL, 2.23 mmol) was stirred at room temperature overnight. The solvent was removed under reduced pressure to give a crude mixture which was purified via column chromatography with silica gel, eluting with methylene chloride/methanol (95/5) to give the title compound (66% yield) as an E/Z isomeric mixture. 1H NMR (CDCl3) δ 9.00 (m, 1H), 8.23 (s, 1H), 8.08 (m, 1H), 7.80 (m, 1H), 7.50 (d, 1H). Mass Spectrum (LCMS, ESI) calculated for C22H22N3O2 372.2 (M+H); found 372.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855722B2
出典データセットuspto-grants-2005_02
ORD IDord-5295c85a8b2c4c4dba4df1e47b34415b
出典メモuspto-grants-2005_02