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HRID 1644967作成日:2026年10月25日

Diisopropylethylamine → (R)-ethyl 4-(4-((6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzoate

https://huagongshe.com/reaction/1644967

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Ethyl 4-(piperazin-1-yl)benzoateHCID 2761178—
反応物(Cyanomethyl)trimethylphosphanium iodideHCID 10514344—
反応物(R)-3-(hydroxymethyl)-6a,7,9,10-tetrahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazin-6(5H)-oneHCID 58324367—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒PropionitrileHCID 7854—
生成物(R)-ethyl 4-(4-((6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzoateHCID 5832446782%

反応条件

温度90 °C

反応手順

To a suspension of (R)-3-(hydroxymethyl)-6a,7,9,10-tetrahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazin-6(5H)-one (333 mg, 1.325 mmol) in propiononitrile (3313 μl) was added (cyanomethyl)trimethylphosphonium iodide (386 mg, 1.590 mmol) and DIPEA (694 μl, 3.98 mmol) and finally ethyl 4-(piperazin-1-yl)benzoate (310 mg, 1.325 mmol). The vial was heated to 90° C. for 12 hours. The reaction was then cooled to room temperature, diluted with EtOH (8 ml) and water (1 mL), then filtered. The precipitate was filtered off and dried in vacuum to afford the title compound 508 mg, 82%) as a white solid. [M+H] calc'd for C24H29N5O3S, 468. found, 468.

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-1e9182c18e6a4922b1594c4ccfb329d1
出典メモuspto-grants-2012_02