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4-Methylphenylhydrazine monohydrochloride → ethyl 8-methyl-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Methylphenylhydrazine monohydrochloride | HCID 12504 | — |
| 反応物 | Ethyl 4-oxo-1-piperidinecarboxylate | HCID 34767 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | ethyl 8-methyl-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylate | HCID 2937007 | 86% |
反応手順
Following a literature procedure (Harbert et al., 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09446022B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-eeda6d7f8cf34dcd8cb745bacce6b560 |
| 出典メモ | uspto-grants-2016_09 |