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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280272Generated: October 31, 2026

Ammonium formate → 3-[5-(4-aminophenyl)-1-(4-carbamoyl-2-methylphenyl)-1H-pyrrol-2-yl]propanoic acid ethyl ester

https://huagongshe.com/reaction/2280272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant3-[1-(4-carbamoyl-2-methyl-phenyl)-5-(nitro-phenyl)-1H-pyrrole-2-yl]-propanoic acid ethyl esterHCID 67178952—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-[5-(4-aminophenyl)-1-(4-carbamoyl-2-methylphenyl)-1H-pyrrol-2-yl]propanoic acid ethyl esterHCID 58305623—

Reaction Steps

3-[1-(4-carbamoyl-2-methyl-phenyl)-5-(nitro-phenyl)-1H-pyrrole-2-yl]-propanoic acid ethyl ester (83 mg, 0.2 mmol) was dissolved in 2 mL methanol under an inert atmosphere of nitrogen. To this solution was added ammonium formate (117 mg, 1.8 mmol) and 10% Pd/C (10 mg). After 24 hrs, the reaction mixture was filtered using celite, rinsed with MeOH and concentrated in vacuo. The residue was diluted with acetone, filtered and the filtrate concentrated in vacuo to give the crude product, which was purified using preparative TLC (solvent: 5% IPA/CH2Cl2). The band corresponding to 3-[5-(4-aminophenyl)-1-(4-carbamoyl-2-methylphenyl)-1H-pyrrol-2-yl]-propanoic acid ethyl ester (Rf=0.6) was isolated and dried under high vacuum (36 mg, 77%, light orange hydroscopic powder).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09138427B2
Source datasetuspto-grants-2015_09
ORD IDord-3ca05ccbd7774517b74e21f4d415656d
Source noteuspto-grants-2015_09