HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734627Generated: October 30, 2026
Ammonium Hydroxide → 4-(4-aminophenyl)-1H-pyrrole-3-carboxamide
https://huagongshe.com/reaction/734627
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | ethyl 4-(4-aminophenyl)-1H-pyrrole-3-carboxylate | HCID 69064082 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(4-aminophenyl)-1H-pyrrole-3-carboxamide | HCID 45116761 | — |
Reaction Steps
A suspension of 0.07 g (0.304 mmol) of ethyl 4-(4-aminophenyl)-1H-pyrrole-3-carboxylate in 10 cm3 of a 22% aqueous ammonium hydroxide solution is heated in an autoclave at a temperature in the region of 80° C. for 84 hours. After stopping the heating and then returning to ambient temperature and pressure, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) to give an orange solid which is purified by flash chromatography [eluent: dichloromethane/methanol/acetonitrile (98/1/1 by volume)]. After concentrating the fractions under reduced pressure, a residue is obtained which is stirred in 10 cm3 of diethyl ether and then filtered and dried under reduced pressure (2.7 kPa) to give 0.02 g of 4-(4-aminophenyl)-1H-pyrrole-3-carboxamide, in the form of a brown solid: EI: m/z=201 (M+) base peak, m/z=185 (M−NH2+), m/z=157 (M-CONH2+).
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-f19f91335b8d43d78963a6916eb2069f |
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| Source note | uspto-grants-2009_09 |
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