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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698912Generated: October 26, 2026

methyl 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylate → methyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1698912

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylateHCID 18322358—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Productmethyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylateHCID 18322367100%

Reaction Steps

A mixture of methyl 5-tert-butyl-3-nitropyrrole-2-carboxylate (0.014 g, 0.062 mmol) and 10% Pd/C (3 mg) in dry MeOH (1 mL) was successively evacuated and purged with H2 three times, then shaken under an atmosphere of H2 (35 psi) for 1 h, diluted with CH2Cl2 and filtered through a pad of Celite®. The filtrate was concentrated under reduced pressure to give methyl 3-amino-5-tert-butylpyrrole-2-carboxylate as a bright yellow oil (0.012 g, 100%). 1H NMR (CDCl3) δ1.26 (s, 9H), 3.82 (s, 3H), 5.52 (d, J=2.8 Hz, 1H), 7.89 (br s, 2H). This material was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344476B1
Source datasetuspto-grants-2002_02
ORD IDord-9ed61ba318064bc58cbbdf6a8ad0925c
Source noteuspto-grants-2002_02