戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 77409作成日:2026年10月24日

Potassium Phosphate, Tribasic → 6-(1,4-Diazabicyclo[3.2.2]nonan-4-yl)-3-methylthieno[2,3-d]pyrimidin-4(3H)-one

https://huagongshe.com/ja/reaction/77409

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物L-ProlineHCID 145742—
反応物1,4-Diazabicyclo(3.2.2)nonaneHCID 398407—
反応物6-bromo-3-methylthieno[2,3-d]pyrimidin-4(3H)-oneHCID 68160197—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒Acetic AcidHCID 176—
溶媒Dimethyl SulfoxideHCID 679—
溶媒MethanolHCID 887—
生成物6-(1,4-Diazabicyclo[3.2.2]nonan-4-yl)-3-methylthieno[2,3-d]pyrimidin-4(3H)-oneHCID 681600972.1%

反応条件

温度90 °C

反応手順

A mixture of 6-bromo-3-methylthieno[2,3-d]pyrimidin-4(3H)-one (70 mg, 0.28 mmol), copper(I) iodide (13.6 mg, 0.071 mmol), L-proline (16.4 mg, 0.143 mmol), 1,4-diazabicyclo[3.2.2]nonane (54.1 mg, 0.428 mmol) and potassium phosphate (132 mg, 0.571 mmol) in DMSO (1 mL) was heated at 90° C. in a sealed vessel for 3 days. The reaction was acidified with acetic acid, diluted with methanol and purified on a scx cartridge (1 g), further purified by acid prep HPLC, passed through a scx cartridge (500 mg) and evaporated to dryness to afford 6-(1,4-Diazabicyclo[3.2.2]nonan-4-yl)-3-methylthieno[2,3-d]pyrimidin-4(3H)-one (1.8 mg, 0.006 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841289B2
出典データセットuspto-grants-2014_09
ORD IDord-577e0f506d014acb9049cec4c76da0ea
出典メモuspto-grants-2014_09