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HRID 2077856作成日:2026年10月26日

Triphenyl phosphite → (S)-methyl 4-ethyl-3-methyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine-7-carboxylate

https://huagongshe.com/reaction/2077856

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(S)-methyl 6-((1-ethoxy-1-oxopropan-2-yl)(ethyl)amino)-5-nitronicotinateHCID 58324496—
触媒PlatinumHCID 23939—
触媒Ammonium metavanadateHCID 516859—
溶媒DichloromethaneHCID 6344—
生成物(S)-methyl 4-ethyl-3-methyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine-7-carboxylateHCID 5941679157.3%

反応手順

(S)-methyl 6-((1-ethoxy-1-oxopropan-2-yl)(ethyl)amino)-5-nitronicotinate (1.22 g, 3.92 mmol) was dissolved in dichloromethane (12 mL). To this solution were added triphenyl phosphite (5.0 mg, 16 umol), ammonium metavanadate (50.0 mg, 0.427 mmol) and Pt/C (5% wt., 0.200 g). The reaction mixture was hydrogenated at 100 psi at 25° C. for 18 h. The mixture was filtered through a small pad of celite and the pad was washed with dichloromethane (20 mL). The combined filtrates were concentrated in vacuo and crystallized with ethyl ether (50 mL) to afford the title compound as a white solid (0.560 g, 57%). [M+H] calc'd for C12H5N3O3, 250; found, 250.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07928105B2
出典データセットuspto-grants-2011_04
ORD IDord-57f4d8d1afb74920ba819c3ef1cde15a
出典メモuspto-grants-2011_04