戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 593449作成日:2026年10月24日

(Pyrimidin-5-yl)boronic acid → (1E,4E)-2-amino-N,N-dipropyl-8-(pyrimidin-5-yl)-3H-benzo[b]azepine-4-carboxamide

https://huagongshe.com/ja/reaction/593449

反応式

関与物質

役割名称HCID仕込み量
反応物(Pyrimidin-5-yl)boronic acidHCID 2795193—
反応物Sodium 2'-(dicyclohexylphosphino)-2,6-dimethoxybiphenyl-3-sulfonateHCID 23677046—
反応物(1E,4E)-2-amino-8-bromo-N,N-dipropyl-3H-benzo[b]azepine-4-carboxamideHCID 66961446—
溶媒Acetonitrile--water (1/1)HCID 18373917—
生成物(1E,4E)-2-amino-N,N-dipropyl-8-(pyrimidin-5-yl)-3H-benzo[b]azepine-4-carboxamideHCID 50905000—

反応手順

The title compound was prepared by the procedure as described in Example 124 (Step F) using (1E,4E)-2-amino-8-bromo-N,N-dipropyl-3H-benzo[b]azepine-4-carboxamide, pyrimidin-5-ylboronic acid, and sodium 2′-(dicyclohexylphosphino)-2,6-dimethoxybiphenyl-3-sulfonate in H2O-MeCN. MS APCI (+) m/z 364 (M+1) detected; 1H-NMR (400 MHz, CDCl3) d 9.21 (s, 111), 9.01 (s, 2H), 7.50 (s, 1H), 7.43 (d, 1H), 7.27-7.29 (m, 1H), 6.84 (s, 1H), 3.47 (br s, 4H), 2.84 (s, 2H), 1.63-1.72 (m, 4H), 0.94 (t, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242964B2
出典データセットuspto-grants-2016_01
ORD IDord-80657666fbf44dfdba1c4b7bbf45c39a
出典メモuspto-grants-2016_01