HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352815Generated: November 1, 2026
4-(4-Methylpiperazin-1-yl)aniline → 5-Acetyl-thiophene-2-carboxylic acid [4-(3-{[4-(4-methyl-piperazin-1-yl)-phenylamino]-methylene}-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide
https://huagongshe.com/reaction/2352815
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(4-Methylpiperazin-1-yl)aniline | HCID 737253 | — |
| Reactant | HCID 178466654 | HCID 178466654 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Acetyl-thiophene-2-carboxylic acid [4-(3-{[4-(4-methyl-piperazin-1-yl)-phenylamino]-methylene}-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide | HCID 73224482 | 57% |
Reaction Steps
A small screw cap test tube was charged with 5-Acetyl-thiophene-2-carboxylic acid [4-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (as prepared in Example 34, 40 mg, 0.093 mmol) and THF (2 mL). To the resulting solution was added 4-(4-methyl-piperazin-1-yl)-phenylamine (22 mg, 0.1150 mmol), and the mixture was stirred for 24 h at 65° C. Subsequently, the reaction mixture was cooled to room temperature and concentrated in vacuo. The solid residue was recrystallized with 2 mL of i-prOH affording the title compound in 57% yield (0.032 g, 0.0528 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07749530B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-1f4e0511ceb344879f8fdfa3bcad70dc |
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| Source note | uspto-grants-2010_07 |
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