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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489996Generated: October 30, 2026

ethyl 1-methyl-5-nitro-1H-indole-2-carboxylate → Ethyl 5-amino-1-methyl-1H-indole-2-carboxylate

https://huagongshe.com/reaction/489996

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 1-methyl-5-nitro-1H-indole-2-carboxylateHCID 10538482—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductEthyl 5-amino-1-methyl-1H-indole-2-carboxylateHCID 11424506—

Reaction Steps

Preferred alternative B. A mixture of ethyl 1-methyl-5-nitro-1H-indole-2-carboxylate (150.0 g), from step (a) or commercial sources, and 10% palladium on carbon catalyst (50% wet) (15.0 g) in ethyl acetate (1800 mL) was hydrogenated at 3 bar at 30° C. for 8 hours. The mixture was then filtered and the solids washed with ethyl acetate (300 mL). The combined filtrate and washings were partially azeotropically dried at reflux and then concentrated to 800 mL to give a solution of product ethyl 5-amino-1-methyl-1H-indole-2-carboxylate in ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979692B2
Source datasetuspto-grants-2005_12
ORD IDord-ff1b539e4f674ef1b36469a1c924f74c
Source noteuspto-grants-2005_12