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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489995Generated: October 30, 2026

Ammonium formate → Ethyl 5-amino-1-methyl-1H-indole-2-carboxylate

https://huagongshe.com/reaction/489995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactantethyl 1-methyl-5-nitro-1H-indole-2-carboxylateHCID 10538482—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthyl 5-amino-1-methyl-1H-indole-2-carboxylateHCID 1142450686%

Reaction Conditions

Temperature20 °C

Reaction Steps

Alterative A. To a mixture of ethyl 1-methyl-5-nitro-1H-indole-2-carboxylate (420 g), from step (a) or commercial sources, and 10% palladium on carbon catalyst (50% wet) (42 g) in ethanol (4200 mL) was added a solution of ammonium formate (541.5 g) in demineralized water (840 mL) at between 25-35° C. over 3 hours. The mixture was stirred for 18 hours at 20° C., and then filtered, washing the solids with ethanol (2100 mL). The combined filtrate and washings were concentrated to 840 mL under vacuum at about 20° C. The resulting slurry was granulated at 5° C., filtered, washed with chilled ethanol (420 mL), and dried to give product ethyl 5-amino-1-methyl-1H-indole-2-carboxylate (316.5 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979692B2
Source datasetuspto-grants-2005_12
ORD IDord-483f21d919f34323b7790f4e86ee42f2
Source noteuspto-grants-2005_12