HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734632Generated: October 30, 2026
HCID 86621475, compound → HCID 86621474, compound
https://huagongshe.com/reaction/734632
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86621475 | HCID 86621475 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86621474 | HCID 86621474 | 61.4% |
Reaction Steps
0.23 g (0.834 mmol) of 2-formylamino-4-(4-nitrophenyl)-1H-pyrrole-3-carboxamide is added at a temperature in the region of 25° C. to a suspension of 0.030 g (0.0285 mmol) of 10% palladium on carbon in 15 cm3 of methanol. After hydrogenation for 5 hours in an autoclave under 2 bar of hydrogen, at a temperature in the region of 25° C., the reaction mixture is filtered, the catalyst is rinsed with three times 5 cm3 of methanol and then the filtrate is concentrated to dryness under reduced pressure (2.7 kPa) to give 0.125 g of 2-formylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamide, in the form of a green solid. 1H NMR (400 MHz, (CD3)2SO, —δ in ppm) 5.13 (broad s, 2H); 5.43 (broad m, 1H); 6.27 (d, J=2.5 Hz, 1H); 6.60 (d, J=9.0 Hz, 2H); 6.80 (broad m, 1H); 6.99 (d, J=9.0 Hz, 2H); 8.34 (d, J=1.5 Hz, 1H); 10.9 (broad s, 1H); 11.25 (broad s, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592365B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-6d378c9517c5448ba068c7eb8cf7061e |
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| Source note | uspto-grants-2009_09 |
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