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HRID 2077902作成日:2026年10月25日

Potassium Carbonate → (R)-methyl 6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazine-3-carboxylate

https://huagongshe.com/reaction/2077902

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Methyl 6-chloro-5-nitronicotinateHCID 346961—
反応物(R)-thiomorpholine-3-carboxylic acidHCID 1152541—
触媒Triphenyl phosphiteHCID 7540—
触媒PlatinumHCID 23939—
触媒Ammonium metavanadateHCID 516859—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-methyl 6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazine-3-carboxylateHCID 5832449752%

反応手順

To a suspension of (R)-thiomorpholine-3-carboxylic acid (1.009 g, 6.86 mmol) in THF was added methyl 6-chloro-5-nitronicotinate (1.35 g, 6.23 mmol) and potassium carbonate (2.58 g, 18.70 mmol). The suspension was heated to reflux for 3 hours. The crude orange solution was allowed to cool to RT and filtered through a pad of celite which was washed with DCM (50 mL), and transferred to a bomb hydroginator. To the solution was added triphenyl phosphite (0.019 ml, 0.061 mmol), platinum (0.238 g, 0.061 mmol), and ammonium metavanadate. The vessel was sealed and pressurized to 140 psi with stirring for 24 h at room temperature. The vessel was depressurized and the mixture was diluted with DCM (100 mL) and refluxed for 30 minutes. The hot mixture was filtered through celite and concentrated to yield 887 mg (52%) of the product as a white solid. [M+H] calc'd for C12H13N3O3S, 280; found, 280.

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-ee95950f0704451bafcec53547580f32
出典メモuspto-grants-2011_04