戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 397088作成日:2026年10月25日

Sodium Acetate → 2-(4-Imidazol-1-yl-benzyl)-1-[4-(2-pyrrolidin-1-yl-ethoxy)phenyl]-1,2,3,4-tetrahydroisoquinolin-6-ol

https://huagongshe.com/reaction/397088

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium AcetateHCID 517045—
反応物4-(1H-imidazol-1-yl)benzaldehydeHCID 736530—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物1-[4-(2-Pyrrolidin-1-yl-ethoxy)phenyl]-1,2,3,4-tetrahydroisoquinolin-6-olHCID 18172449—
溶媒MethanolHCID 887—
生成物2-(4-Imidazol-1-yl-benzyl)-1-[4-(2-pyrrolidin-1-yl-ethoxy)phenyl]-1,2,3,4-tetrahydroisoquinolin-6-olHCID 18172391112.3%

反応手順

A solution of 1-[4-(2-pyrrolidin-1-yl-ethoxy)phenyl]-1,2,3,4-tetrahydroisoquinolin-6-ol (0.023 g, 0.067 mmol), 4-imidazol-1-yl-benzaldehyde (0.011 g, 0.063 mmol), NaOAc (0.011 g, 0.14 mmol), and sodium cyanoborohydride (0.004 g, 0.063 mmol) in MeOH (2.0 ml) was stirred at rt for 18 hr. The reaction mixture was evaporated in vacuo to a yellow residue that was dissolved in EtOAc (5 ml) and washed first with sat. NaHCO3 solution (5 ml) and then with H2O (5 ml). The organic solution was dried over MgSO4 and evaporated to give 0.035 g of yellow residue. Purification by preparative TLC, eluting with EtOAc:MeOH (7:3), gave 0.007 g (23% yield) of white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06608203B2
出典データセットuspto-grants-2003_08
ORD IDord-ca3227ff177140879ce3c5041d487307
出典メモuspto-grants-2003_08