戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 80765作成日:2026年10月24日

Methyl 4-methyl-3-oxopentanoate → 1-(2-(2,6-dimethylphenyl)-4-methoxy-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)-4-methylpentane-1,3-dione

https://huagongshe.com/ja/reaction/80765

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-methyl-3-oxopentanoateHCID 2759969—
反応物2-(2,6-Dimethylphenyl)-4-methoxy-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidineHCID 71244699—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒TolueneHCID 1140—
生成物1-(2-(2,6-dimethylphenyl)-4-methoxy-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)-4-methylpentane-1,3-dioneHCID 86690252—

反応条件

温度150 °C

反応手順

A mixture of 2-(2,6-dimethylphenyl)-4-methoxy-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine (4.8 g, 17.82 mmol), methyl 4-methyl-3-oxopentanoate (5.14 g, 35.6 mmol), and DMAP (0.327 g, 2.67 mmol) was dissolved in toluene (70 mL). The mixture was evenly divided into four 20 mL microwave vials. Each vial was heated to 150° C. for 30 min via microwave irradiation. The reaction mixtures were combine and directly concentrated. The resulting residue was purified via silica gel FCC (0-80% EtOAc/heptane) to give 1-(2-(2,6-dimethylphenyl)-4-methoxy-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)-4-methylpentane-1,3-dione. MS (ESI+) m/z 382.3 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846656B2
出典データセットuspto-grants-2014_09
ORD IDord-2d40f3e3235141af880e9afa258ab03e
出典メモuspto-grants-2014_09