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HRID 640990作成日:2026年10月25日
Tetrahydrofuran → 5-chloro-1-methyl-N-[3-[3-[[4-(4-methylpiperazin-1-yl)anilino]methylidene]-2-oxo-1H-indole-6-carbonyl]phenyl]pyrazole-4-carboxamide
https://huagongshe.com/reaction/640990
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 4-(4-Methylpiperazin-1-yl)aniline | HCID 737253 | — |
| 反応物 | HCID 178481853 | HCID 178481853 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 5-chloro-1-methyl-N-[3-[3-[[4-(4-methylpiperazin-1-yl)anilino]methylidene]-2-oxo-1H-indole-6-carbonyl]phenyl]pyrazole-4-carboxamide | HCID 178480717 | 71% |
反応手順
A small screw cap test tube was charged with 5-Chloro-1-methyl-1H-pyrazole-4-carboxylic acid [3-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (prepared below, 100 mg, 0.237 mmol) and THF (2.5 mL). To the resulting solution was added 4-(4-methyl-piperazin-1-yl)-phenylamine (59.2 mg, 0.309 mmol), and the mixture was stirred for 24 h at 65° C. Subsequently, the reaction mixture was cooled to room temperature and diluted with EtOAc (5 mL) and Hexanes (40 mL). The precipitate that formed was then filtered and washed with acetone (5 mL) to afford the title compound in 71% yield (0.100 g, 0.168 mmol).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07692005B2 |
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| 出典データセット | uspto-grants-2010_04 |
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| ORD ID | ord-201069fda86b42358b0f52a58be54e5c |
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| 出典メモ | uspto-grants-2010_04 |
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