戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 18294作成日:2026年10月24日

Nitrogen → tert-butyl (E)-3-(8-oxo-6,7,8,9-tetrahydro-5H-pyrido[2,3-b]azepin-3-yl)acrylate

https://huagongshe.com/ja/reaction/18294

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物tert-Butyl acrylateHCID 15458—
反応物Tri-o-tolylphosphineHCID 80271—
反応物DiisopropylethylamineHCID 81531—
反応物3-Bromo-5,6,7,9-tetrahydro-pyrido[2,3-b]azepin-8-oneHCID 22139024—
触媒palladium(II) acetateHCID 167845—
溶媒PropionitrileHCID 7854—
生成物tert-butyl (E)-3-(8-oxo-6,7,8,9-tetrahydro-5H-pyrido[2,3-b]azepin-3-yl)acrylateHCID 2357446558.5%

反応手順

A solution of 3-bromo-5,6,7,9-tetrahydro-pyrido[2,3-b]azepin-8-one (1.00 g, 4.15 mmole), tert-butyl acrylate (0.67 mL, 4.60 mmole), DIEA (1.45 mL, 8.30 mmole), Pd(OAc)2 (0.09 g, 0.42 mmole) and P(o-tol)3 (0.25 g, 0.85 mmole) in propionitrile (25 mL) was purged with N2 and then heated at reflux 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 (ethyl acetate). The title compound (0.70 g, 58%) was obtained as a light yellow solid after drying in vacuo: MS (ES) m/e 289 (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-46a636f3225d4cfa8d382d5ef383e8e6
出典メモuspto-grants-2010_06