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HRID 520698作成日:2026年10月25日
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-(4-((2-aminopyridin-4-yl)oxy)phenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide
https://huagongshe.com/reaction/520698
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| 反応物 | HOAt | HCID 181649 | — |
| 反応物 | Antipyric acid | HCID 246564 | — |
| 反応物 | HCID 22936741 | HCID 22936741 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(4-((2-aminopyridin-4-yl)oxy)phenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide | HCID 73053608 | 53% |
反応手順
To a mixture of 4-(4-aminophenoxy)pyridin-2-amine (101 mg, 0.5 mmol) and 1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylic acid (118 mg, 0.51 mmol) in DCM (5 mL) was added EDCI (115 mg, 0.6 mmol) and HOAT (13.6 mg, 0.1 mmol). The reaction was stirred at 45° C. for 3 hours, and then quenched with water (20 mL). The organic phase was separated and concentrated in vacuo. The residue was purified by a silica gel column chromatography (DCM/CH3OH (v/v)=20/1) to give the title compound as a light grey solid (110 mg, 49.2%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09326975B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-c3d8185e6f914b71bc3d284cc4854abf |
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| 出典メモ | uspto-grants-2016_05 |
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