戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2051032作成日:2026年10月27日

Water → 7-Methyl-2,3-dihydro-1H-pyrrolo[1,2-a] benzimidazole-5,8-dione

https://huagongshe.com/reaction/2051032

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Potassium BromideHCID 253877—
反応物Potassium nitrosodisulfonateHCID 3032624—
反応物2,3-Dihydro-5-amino-7-methyl-1H-pyrrolo[1,2-a]benzimidazoleHCID 15661171—
溶媒Chloroform methanolHCID 21584188—
生成物7-Methyl-2,3-dihydro-1H-pyrrolo[1,2-a] benzimidazole-5,8-dioneHCID 10219860—

反応手順

To a suspension of 218 mg (0.83 mmol) of 25 in 10 mL of water, containing 200 mg of monobasic potassium phosphate, was added a solution of 1.34 g of Fremy's salt in 50 mL of water containing 500 mg of monobasic potassium phosphate. The reaction mixture was stirred at room temperature for 2 hours and extracted with 3×50 mL portions of chloroform. The dried extracts (sodium sulfate) were concentrated and then chromatographed over silica gel, employing chloroform as the eluant, to afford yellow-colored 26, 105 mg (61%) yield. Recrystallization from chloroform/hexane afforded analytically pure 26: mp 162°-164° C.; TLC (methanol chloroform[10:90]), Rf =0.62; IR(KBr pellet) 1675, 1659, 1647, 1515, 1154 cm-1 ; 1H NMR (dimethyl sulfoxide-d6) δ6.54 (1 H, quartet, J=1.6 Hz, C(6) proton coupled to 7-methyl), 4.16 (2 H, t, J~7 Hz, C(1) methylene), 2.86 (2 H, t, J~7 Hz, C(3) methylene), 2.62 (2 H, quintet, J~7 Hz, C(2) methylene), 2.00 (3 H, d, J=1.6 Hz, 7-methyl coupled to C(6) proton); mass spectrum (EI mode) m/z 202 (P+), 174 (P+ -CO), 146 (P+ -2CO), Anal. Calcd for C11H10N2O2 : C, 65.33; H, 4.98; N, 13.85. Found: C, 65.15; H, 4.70; N, 13.61.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05015742
出典データセットuspto-grants-1991_05
ORD IDord-f3c60b16a6624fcc932e8046247f075c
出典メモuspto-grants-1991_05