戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1182239作成日:2026年10月26日

1,1'-Carbonyldiimidazole → methyl 4-bromo-2-{[(5-methoxy-2-methyl-1H-indol-3-yl)acetyl]amino}benzoate

https://huagongshe.com/reaction/1182239

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物5-Methoxy-2-methylindole-3-acetic acidHCID 76151—
反応物Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
反応物Methyl 2-Amino-4-bromobenzoateHCID 17871390—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物methyl 4-bromo-2-{[(5-methoxy-2-methyl-1H-indol-3-yl)acetyl]amino}benzoateHCID 6935432566.6%

反応手順

5-Methoxy-2-methyl-3-indole acetic acid (5 g, obtainable from Acros), carbonyidiimidazole (4.44 g) and tetrahydrofuran (120 ml) were stirred at room temperature for 30 min after which methyl 4-bromoanthranilate (5.24 g) and pyridinium tosylate (13.69 g) were added and the mixture refluxed for 14 h. After diluting with dichloromethane (200 ml), the residue was washed with 2M hydrochloric acid (200 ml), 2M sodium hydroxide (200 ml), water (200 ml) and brine (200 ml) and dried (MgSO4). After solidifying by treatment with cyclohexane and ethyl acetate, the solid was triturated with ether to afford methyl 4-bromo-2-{[(5-methoxy-2-methyl-1H-indol-3-yl)acetyl]amino}benzoate (6.54 g), MH+ 433, 435; MH− 431, 433; TR 3.67 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07288564B2
出典データセットuspto-grants-2007_10
ORD IDord-b71ed51311ea431bae8aa2e80406c250
出典メモuspto-grants-2007_10