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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394817Generated: November 3, 2026

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

https://huagongshe.com/reaction/1394817

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 numberUS07348355B2
Source datasetuspto-grants-2008_03
ORD IDord-4bf4887d72ce48379161c959e21673a1
Source noteuspto-grants-2008_03