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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactantethyl 4-(4-aminophenyl)-1H-pyrrole-3-carboxylateHCID 69064082—
SolventDiethyl EtherHCID 3283—
Product4-(4-aminophenyl)-1H-pyrrole-3-carboxamideHCID 45116761—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592365B2
Source datasetuspto-grants-2009_09
ORD IDord-f19f91335b8d43d78963a6916eb2069f
Source noteuspto-grants-2009_09