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HRID 716313作成日:2026年10月24日

Potassium Sodium Tartrate → (S)-3-(hydroxymethyl)-7,8-dihydro-5H-azeto[1,2-a]pyrido[3,2-e]pyrazin-6(6aH)-one

https://huagongshe.com/ja/reaction/716313

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Sodium TartrateHCID 9357—
反応物Sodium hydrideHCID 24758—
反応物Aluminium lithium hydrideHCID 21226445—
反応物(S)-methyl 6-oxo-6,6a,7,8-tetrahydro-5H-azeto[1,2-a]pyrido[3,2-e]pyrazine-3-carboxylateHCID 58324364—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-3-(hydroxymethyl)-7,8-dihydro-5H-azeto[1,2-a]pyrido[3,2-e]pyrazin-6(6aH)-oneHCID 5832437266.2%

反応手順

(S)-methyl 6-oxo-6,6a,7,8-tetrahydro-5H-azeto[1,2-a]pyrido[3,2-e]pyrazine-3-carboxylate (0.570 g, 2.444 mmol) was suspended in Tetrahydrofuran (Volume: 8.15 ml) under nitrogen atmosphere and NaH (196 mg, 4.9 mmol) was added in several portions over 2 min. The reaction mixture was stirred at room temperature for 10 min and cooled to below −50° C. lithium aluminum hydride (2.200 ml, 4.40 mmol) was added over the period of 5 min and the reaction was kept at a temperature between −30 and −20° C. for 1 h (LCMS: >95% conversion). The mixture was cooled to below −50° C. and MeOH (4 mL) was added. Water (1 mL) was added and the reaction mixture was stirred at rt for 10 min. Rochelle salt (20% solution) was added (10 mL) and the mixture was extracted with EtOAc (3×30 mL) and THF (3×100 mL). The combined organic extracts were dried (Na2SO4 and MgSO4), filtered and concentrated in vacuo. The residue was suspended in THF/Ethyl ether (1:1, 20 mL), filtered off and dried in vacuum to afford (S)-3-(hydroxymethyl)-7,8-dihydro-5H-azeto[1,2-a]pyrido[3,2-e]pyrazin-6(6aH)-one (0.332 g, 1.618 mmol, 66.2% yield) as a light tan solid. [M+H] calc'd for C10H11N3O2, 205. found, 205.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09187497B2
出典データセットuspto-grants-2015_11
ORD IDord-600a13bcfdc94a299c2b1105d7d89434
出典メモuspto-grants-2015_11