戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 44487作成日:2026年10月24日

Cesium carbonate → 2-methyl-6-(4-morpholinyl)-1-(1-naphthalenylmethyl)-4-(1H-pyrazol-5-yl)-1H-benzimidazole

https://huagongshe.com/ja/reaction/44487

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Tris(1,1-dimethylethyl)phosphineHCID 83681—
反応物1H-Pyrazole-5-boronic acidHCID 11251979—
反応物4-bromo-2-methyl-6-(4-morpholinyl)-1-(1-naphthalenylmethyl)-1H-benzimidazoleHCID 66977050—
触媒(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物2-methyl-6-(4-morpholinyl)-1-(1-naphthalenylmethyl)-4-(1H-pyrazol-5-yl)-1H-benzimidazoleHCID 56959533—

反応条件

温度100 °C

反応手順

A mixture of 4-bromo-2-methyl-6-(4-morpholinyl)-1-(1-naphthalenylmethyl)-1H-benzimidazole (200 mg, 0.46 mmol), 1H-pyrazol-5-ylboronic acid (100 mg, 0.92 mmol), Pd(dba)2 (40 mg, 0.046 mmol), Cs2CO3 (300 mg, 0.92 mmol) and P(t-Bu)3 (10 wt % in hexane, 20 mg, 0.092 mmol) in dioxane (20 mL) and water (10 mL), was stirred at 100° C. for 18 h under a nitrogen atmosphere. The reaction mixture was cooled and then concentrated. The resulting residue was purified by silica gel chromatography eluted with EtOAc to give the product (140 mg 72%), as a white solid. 1H NMR showed this compound is in a form of tautomeric mixture (major tautomer/minor tautomer=5/3) 1H NMR of the major tautomer (300 MHz, DMSO-d6) δ ppm 2.45 (s, 3H), 3.08 (s, 4H), 3.71 (s, 4H), 6.00 (s, 2H), 6.37 (d, 1H, J=7.2 Hz), 6.96 (s, 1H), 7.24-7.72 (m, 6H), 7.83-7.87 (m, 1H), 8.01 (d, 1H, J=7.2 Hz), 8.25 (d, 1H, J=4.2 Hz), 13.24 (br s, 1H); LC-MS: m/e=424 [M+1]+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541411B2
出典データセットuspto-grants-2013_09
ORD IDord-80df6bc6513e44e0aac1ed53c86459f0
出典メモuspto-grants-2013_09