HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227669Generated: October 29, 2026
HCID 57756882, compound → HCID 57756892, compound
https://huagongshe.com/reaction/227669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57756882 | HCID 57756882 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57756892 | HCID 57756892 | 99.2% |
Reaction Steps
To a suspension of 0.024 g (0.222 mmol) of 10% palladium-on-charcoal in 63 cm3 of methanol is added, at a temperature in the region of 20° C., 0.331 g (0.956 mmol) of 4-tert-butyloxycarbonylamino-3-(4-nitrophenyl)-1H-pyrrole-2-carboxamide. After hydrogenating for 5 hours in an autoclave under 4 bar of hydrogen, at a temperature in the region of 40° C., the reaction mixture is filtered. The catalyst is rinsed with twice 15 cm3 of methanol and the filtrate is then concentrated to dryness under reduced pressure (2.7 kPa) to give 0.3 g of 4-tert-butyloxycarbonylamino-3-(4-aminophenyl)-1H-pyrrole-2-carboxamide in the form of a white solid melting at about 142° C.; EI: m/z=316 M+; m/z=260 [M-tBu]+; m/z=243 [M-OtBu]+; m/z=199 [243-CONH2]+; m/z=57: [tBu]+ base peak.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560571B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-e90493ea6b544f308ad68629e03e3587 |
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| Source note | uspto-grants-2009_07 |
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