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HRID 79577作成日:2026年10月23日

Acetic Acid → tert-butyl 4-(5-(2-acetylhydrazinecarbonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazine-1-carboxylate

https://huagongshe.com/ja/reaction/79577

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
反応物tert-Butyl 4-(5-(hydrazinecarbonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazine-1-carboxylateHCID 68759320—
溶媒Acetonitrile tetrahydrofuranHCID 22177404—
生成物tert-butyl 4-(5-(2-acetylhydrazinecarbonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazine-1-carboxylateHCID 6876210372%

反応手順

Ethyl 2-ethoxyquinoline-1(2H)-carboxylate (226 mg, 0.916 mmol) was added to acetic acid (50.0 mg, 0.832 mmol) in THF/ACN (5 mL), and the reaction was stirred at room temperature for 1 hour. tert-Butyl 4-(5-(hydrazinecarbonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazine-1-carboxylate (300 mg, 0.832 mmol, Example 18) was added, and the reaction was heated to 70° C. for 1 hour. The reaction was then concentrated to dryness. The resulting residue was crystallized from DCM to yield tert-butyl 4-(5-(2-acetylhydrazinecarbonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazine-1-carboxylate (241 mg, 71.9% yield) as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841304B2
出典データセットuspto-grants-2014_09
ORD IDord-7131c0df112d4b0aa02df20b00ba3200
出典メモuspto-grants-2014_09