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HRID 404279作成日:2026年10月25日

4-Methylphenylhydrazine monohydrochloride → ethyl 8-methyl-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylate

https://huagongshe.com/reaction/404279

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methylphenylhydrazine monohydrochlorideHCID 12504—
反応物Ethyl 4-oxo-1-piperidinecarboxylateHCID 34767—
溶媒EthanolHCID 702—
生成物ethyl 8-methyl-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylateHCID 293700786%

反応手順

Following a literature procedure (Harbert, C. A.; Plattner, J. J.; Welch, W. M.; Weissman, A.; Koe, B. K. J. Med. Chem. 1980, 23, 635-643)p-tolylhydrazine hydrochloride (0.500 g, 3.15 mmol) and 1-carbethoxy-4-piperidone (0.18 mL, 1.17 mmol) were suspended in EtOH (0.880 mL) and heated to reflux for 2 hours. The reaction mixture was removed from heat and allowed to stand overnight at ambient temperature. The resulting mixture was filtered and washed with 50% aqueous EtOH to afford the desired product as a beige powder (259 mg, 86%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08748473B2
出典データセットuspto-grants-2014_06
ORD IDord-e13e50a488614e7a999c713a5be124ca
出典メモuspto-grants-2014_06