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HRID 501082作成日:2026年10月24日

Hydrazine → benzyl 4-(6-oxo-6,7-dihydro-5H-imidazo[4,5-c]pyridazin-5-yl)piperidine-1-carboxylate

https://huagongshe.com/ja/reaction/501082

反応式

関与物質

役割名称HCID仕込み量
反応物HydrazineHCID 9321—
反応物Benzyl 4-(5-allyl-2,4-dioxoimidazolidin-1-yl)piperidine-1-carboxylateHCID 22293269—
反応物Sodium periodateHCID 23667635—
触媒Osmium TetroxideHCID 30318—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium SulfiteHCID 24437—
溶媒Sodium BicarbonateHCID 516892—
生成物benzyl 4-(6-oxo-6,7-dihydro-5H-imidazo[4,5-c]pyridazin-5-yl)piperidine-1-carboxylateHCID 222932186.8%

反応条件

温度50 °C

反応手順

Benzyl 4-(5-allyl-2,4-dioxoimidazolidin-1-yl)piperidine-1-carboxylate (0.480 g, 1.34 mmol) was dissolved in THF (5 mL), and osmium tetroxide (0.05 mL, 2.5% solution in t-butanol) was added followed by a solution of sodium periodate (0.862 g, 4.03 mmol) in water (4 mL). After 24 h, the reaction was diluted with saturated aqueous Na2SO3 and NaHCO3 and extracted with ethyl acetate (4×). The combined organic washes were dried over sodium sulfate, filtered and evaporated to give the crude aldehyde (0.352 g). To a portion of this material (0.250 g, 0.696 mmol) in acetic acid (10 mL) was added hydrazine (0.446 mL, 13.9 mmol). This mixture was heated at 50° C. for 24 h, and then concentrated to dryness. Purification by reverse phase HPLC (C-18, 95% water/acetonitrile→5% water/acetonitrile with 0.1% trifluoroacetic acid) gave the product (0.032 g). MS 354.2 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772224B2
出典データセットuspto-grants-2010_08
ORD IDord-bc746a2a1c714039912fafda9466d504
出典メモuspto-grants-2010_08