関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Hydrazine | HCID 9321 | — |
| 反応物 | (4-Methoxyphenyl)hydrazine | HCID 77023 | — |
| 反応物 | (1-Ethoxyethylidene)malononitrile | HCID 79450 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile | HCID 67120041 | 81% |
反応手順
To a stirred solution of 2-(1-ethoxyethylidene)malononitrile (958 mg, 7.04 mmol) in EtOH (12 mL) was added (4-methoxyphenyl)hydrazine (1.12 g, 8.09 mmol). (Prior to using the hydrazine its HCl salt was washed with NaHCO3/CH2Cl2. The organic phase was concentrated and used directly.) The solution was heated to 105° C. in the microwave for 20 minutes. CH2Cl2 was added and the organic phase was washed with 1 M HCl and the organic extract was washed with aqueous NaHCO3. The solution was dried using a phase separator and concentrated under reduced pressure to give 5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile (1.30 g, 81%) which was used as such in the next step. The procedure was adapted from J. Med. Chem. 2004, 47, 5894-5911.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08653112B2 |
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| 出典データセット | uspto-grants-2014_02 |
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| ORD ID | ord-79fa3684f21848b882e7327d35308177 |
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| 出典メモ | uspto-grants-2014_02 |
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