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HRID 1408647作成日:2026年10月25日

3-(Methylcarbamoyl)benzeneboronic acid → 3-(2'-amino-1'-methyl-5'-oxo-2-phenyl-1',5'-dihydrospiro[chroman-4,4'-imidazole]-6-yl)-N-methylbenzamide

https://huagongshe.com/reaction/1408647

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Methylcarbamoyl)benzeneboronic acidHCID 2773524—
反応物2'-amino-6-bromo-1'-methyl-2-phenylspiro[chroman-4,4'-imidazol]-5'(1'H)-oneHCID 58423768—
触媒HCID 178418476HCID 178418476—
溶媒Cesium carbonateHCID 10796—
溶媒1,4-DioxaneHCID 31275—
生成物3-(2'-amino-1'-methyl-5'-oxo-2-phenyl-1',5'-dihydrospiro[chroman-4,4'-imidazole]-6-yl)-N-methylbenzamideHCID 584238264.2%

反応条件

温度120 °C

反応手順

Pd(PPh3)2Cl2 (10 mg) in a 10 mL CEM test tube under Ar was treated sequentially with 2′-amino-6-bromo-1′-methyl-2-phenylspiro[chroman-4,4′-imidazol]-5′(1′H)-one (20 mg, 0.052 mmol) in 1,4-dioxane (1 mL), Cs2CO3 (2 N, 0.3 mL) and 3-(methylcarbamoyl)phenylboronic acid (18.6 mg, 0.104 mmol). The mixture was heated in a microwave reactor at 120° C. for 30 minutes. The reaction mixture was concentrated in vacuo to give the residue, which was purified by preparative TLC and preparative HPLC to give pure 3-(2′-amino-1′-methyl-5′-oxo-2-phenyl-1′,5′-dihydrospiro[chroman-4,4′-imidazole]-6-yl)-N-methylbenzamide (0.96 mg, 4%). 1H-NMR (CDCl3): 2.36 (d, 1H), 2.57 (t, 1H), 2.73 (s, 3H), 2.97 (s, 3H), 5.87 (d, 1H), 7.11 (m, 2H), 7.45 (m, 8H), 7.51 (m, 1H), 7.60 (s, 1H), 7.78 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08921359B2
出典データセットuspto-grants-2014_12
ORD IDord-953ddfc2eaa442a6ac3fe94595e28608
出典メモuspto-grants-2014_12