戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 536098作成日:2026年10月27日

Acetic Acid → Ethyl 3-[(1H-benzimidazol-2-ylmethyl)amino]-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/536098

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物1H-Benzimidazole-2-carboxaldehydeHCID 76826—
反応物Ethyl 3-amino-1H-pyrrole-2-carboxylateHCID 2773439—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒MethanolHCID 887—
生成物Ethyl 3-[(1H-benzimidazol-2-ylmethyl)amino]-1H-pyrrole-2-carboxylateHCID 6706852681.1%

反応手順

A reaction mixture of 3-amino-1H-pyrrole-2-carboxylic acid ethyl ester (0.77 g, 4.99 mmol), 1H-benzoimidazole-2-carboxaldehyde (0.88 g, 5.99 mmol), NaCNBH3 (0.31 g, 4.99 mmol) and HOAc (0.57 mL, 9.99 mmol) in methanol (15 mL) was stirred at r.t. overnight. The mixture was then heated at 50° C. for 5 h. Cooled to r.t. and evaporated in vacuo. The residue was dissolved in ethyl acetate and washed with water. The aqueous phase was extracted with ethyl acetate (twice). The combined organic layers were dried (MgSO4) and concentrated. The crude product was purified by flash column chromatography (heptane/ethyl acetate (1:0 to 0:1), obtaining 1.15 g (81%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08859568B2
出典データセットuspto-grants-2014_10
ORD IDord-6b5f3f91fcb74e599bb6787659d0c083
出典メモuspto-grants-2014_10