戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2092591作成日:2026年10月26日

Tetrahydrofuran → 6-(5-Amino-2-methyl-phenyl)-2-[4-(4-methyl-piperazine-1-carbonyl)phenylamino]-7,8-dihydro-6H-pyrido[4,3-d]pyrimidin-5-one

https://huagongshe.com/reaction/2092591

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物6-(2-Methyl-5-nitro-phenyl)-2-[4-(4-methyl-piperazine-1-carbonyl)phenylamino]-7,8-dihydro-6H-pyrido[4,3-d]pyrimidin-5-oneHCID 67329210—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物6-(5-Amino-2-methyl-phenyl)-2-[4-(4-methyl-piperazine-1-carbonyl)phenylamino]-7,8-dihydro-6H-pyrido[4,3-d]pyrimidin-5-oneHCID 67329058—

反応手順

To a solution of 6-(2-Methyl-5-nitro-phenyl)-2-[4-(4-methyl-piperazine-1-carbonyl)phenylamino]-7,8-dihydro-6H-pyrido[4,3-d]pyrimidin-5-one (100 mg, 0.199 mmol) in the mixed solvent of THF (3 ml) and methanol (3 ml) was added 10% Pd/C, and the reaction mixture was stirred for 12 hours at room temperature under a hydrogen balloon. The reaction mixture was filtered and the filtrate was concentrated under vacuum to give 6-(5-Amino-2-methyl-phenyl)-2-[4-(4-methyl-piperazine-1-carbonyl)-phenylamino]-7,8-dihydro-6H-pyrido[4,3-d]pyrimidin-5-one [23] as a off white solid [Yield: 83.0 mg, 88.3%]

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08440679B2
出典データセットuspto-grants-2013_05
ORD IDord-d95af720ec9a49668072adbf21274d0e
出典メモuspto-grants-2013_05