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HRID 18318作成日:2026年10月25日

Tri-o-tolylphosphine → (E)-N-(1H-indol-3-ylmethyl)-N-methyl-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylamide

https://huagongshe.com/reaction/18318

反応式

関与物質

役割名称HCID仕込み量
反応物Tri-o-tolylphosphineHCID 80271—
反応物DiisopropylethylamineHCID 81531—
反応物6-Bromo-3,4-dihydro-1,8-naphthyridin-2(1H)-oneHCID 11096325—
反応物N-(1H-indol-3-ylmethyl)-N-methylacrylamideHCID 22139147—
触媒palladium(II) acetateHCID 167845—
溶媒PropionitrileHCID 7854—
生成物(E)-N-(1H-indol-3-ylmethyl)-N-methyl-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylamideHCID 1031647637%

反応手順

A solution of 6-bromo-3,4-dihydro-1H-1,8-naphthyridin-2-one (0.64 g, 2.80 mmole), N-(1H-indol-3-ylmethyl)-N-methylacrylamide (0.60 g, 2.80 mmole), Pd(OAc)2 (0.06 g, 0.28 mmole), tri-ortho-tolylphosphine (0.17 g, 0.56 mmole) and diisopropylethylamine (0.73 mL, 4.2 mmole) in propionitrile (50 mL) was deoxygenated, then was heated to reflux under N2 overnight. The dark mixture was filtered through a pad of Celite®, and the filter pad was rinsed with acetonitrile (250 mL). The filtrate was concentrated in vacuo, and the residue was purified by flash chromatography on silica gel (10% MeOH/CHCl3). The title compound (0.37 g, 37%) was obtained as a light yellow solid after drying in vacuo: MS (ES) m/e 361 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741339B2
出典データセットuspto-grants-2010_06
ORD IDord-1395cd279e864ba28644241d779103fc
出典メモuspto-grants-2010_06