HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640880Generated: October 30, 2026
3-Aminophenol → 5-Acetyl-thiophene-2-carboxylic acid (4-{3-[(3-hydroxy-phenylamino)-methylene]-2-oxo-2,3-dihydro-1H-indole-6-carbonyl}-phenyl)-amide
https://huagongshe.com/reaction/640880
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminophenol | HCID 11568 | — |
| Reactant | HCID 178466654 | HCID 178466654 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Acetyl-thiophene-2-carboxylic acid (4-{3-[(3-hydroxy-phenylamino)-methylene]-2-oxo-2,3-dihydro-1H-indole-6-carbonyl}-phenyl)-amide | HCID 73224484 | 64% |
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 3-aminophenol (13 mg, 0.1191 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 64% yield (0.031 g, 0.0592 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07692005B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-c32eb016a6374d5d855273d64f3e8fb8 |
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| Source note | uspto-grants-2010_04 |
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