HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382008Generated: October 27, 2026
Pyrrole-2-carboxaldehyde → (Z)-1,3-dihydro-4-iodo-3-[(1H-pyrrol-2-yl)methylene]-indol-2-one
https://huagongshe.com/reaction/382008
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyrrole-2-carboxaldehyde | HCID 13854 | — |
| Reactant | 4-Iodo-1,3-dihydro-2H-indol-2-one | HCID 10923225 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | (Z)-1,3-dihydro-4-iodo-3-[(1H-pyrrol-2-yl)methylene]-indol-2-one | HCID 15548052 | 65.2% |
Reaction Steps
A mixture of 1,3-dihydro-4-iodo-2H-indol-2-one (404.1 mg, 1.56 mmol) (see Fukuyama et al., supra) and pyrrole-2-carboxaldehyde (163.2 mg, 1.72 mmol) (Aldrich) in 2-propanol (6.2 mL) was treated with 2 drops of piperidine. The reaction mixture was heated at reflux for 24 h and then allowed to cool to 23° C., at which time, the reaction mixture was filtered. The solid was washed several times with cold distilled water and then allowed to air dry to provide pure (Z)-1,3-dihydro-4-iodo-3-[(1H-pyrrol-2-yl)methylene]-2H-indol-2-one (341.8 mg, 65%) as a yellow solid which was used without further purification. (MP 256-258° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06307056B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-9c29a8266a2c433d9a43cbb3abbef0b1 |
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| Source note | uspto-grants-2001_10 |
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