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HRID 716281作成日:2026年10月26日

Triphenyl phosphite → 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/716281

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Ethyl 4-(5-(methoxycarbonyl)-3-nitropyridin-2-yl)thiomorpholine-3-carboxylateHCID 58324448—
反応物HCID 178418361HCID 178418361—
触媒PlatinumHCID 23939—
触媒Ammonium metavanadateHCID 516859—
溶媒DichloromethaneHCID 6344—
生成物Methyl 6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazine-3-carboxylateHCID 5832451496%

反応手順

Ethyl 4-(5-(methoxycarbonyl)-3-nitropyridin-2-yl)thiomorpholine-3-carboxylate (600 mg g, 1.69 mmol) was dissolved in dichloromethane (5 mL). To the yellow solution was added ammonium metavanadate (10.0 mg, 0.085 mmol), triphenyl phosphite (aprox 10 ul, 0.032 mmol), and Pt/C (50 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 (20 mL) which was refluxed for 30 min. The hot solution was filtered through a pad of celite and washed with hot dichloromethane (3×10 mL). The filtrate was concentrated to yield the title compound (452 mg, 96%) 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US09187497B2
出典データセットuspto-grants-2015_11
ORD IDord-1f6d616674d8441fbed9df9b2633e448
出典メモuspto-grants-2015_11