戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1644945作成日:2026年10月27日

Triphenyl phosphite → Methyl 4-methyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine-7-carboxylate

https://huagongshe.com/reaction/1644945

反応式

関与物質

役割名称HCID仕込み量
反応物Triphenyl phosphiteHCID 7540—
反応物Methyl 6-((2-methoxy-2-oxoethyl)(methyl)amino)-5-nitronicotinateHCID 58324470—
反応物HCID 178418361HCID 178418361—
触媒PlatinumHCID 23939—
触媒Ammonium metavanadateHCID 516859—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-methyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine-7-carboxylateHCID 5832445568.8%

反応手順

Methyl 6-((2-methoxy-2-oxoethyl)(methyl)amino)-5-nitronicotinate (2.7 g, 9.53 mmol) was dissolved in dichloromethane (10 mL). To the yellow solution was added ammonium metavanadate (30.0 mg, 0.256 mmol), triphenyl phosphite (aprox 30 ul, 0.097 mmol), and Pt/C (300 mg, 5% w/w). The reaction mixture was pressurized with hydrogen gas (110 psi) and stirred at room temperature for 16 h. The reaction was then depressurized and diluted with dichloromethane (100 mL) which was then refluxed for 30 min. The hot solution was filtered through a pad of celite and washed with hot dichloromethane (3×20 mL). The filtrate was concentrated in vacuo to yield the title compound (1.45 g, 68%) as a white solid. [M+H] calc'd for C10H11N3O3, 222. found, 222.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124606B2
出典データセットuspto-grants-2012_02
ORD IDord-dc1e4c133264475eb51f19e85d4d66e5
出典メモuspto-grants-2012_02