HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394816Generated: November 2, 2026
Ammonium formate → Ethyl 5-amino-1-methyl-1H-indole-2-carboxylate
https://huagongshe.com/reaction/1394816
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | ethyl 1-methyl-5-nitro-1H-indole-2-carboxylate | HCID 10538482 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 5-amino-1-methyl-1H-indole-2-carboxylate | HCID 11424506 | 86% |
Reaction Steps
Alternative 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07348355B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-eeec3f22ffda4f8c81b2c67744ca432d |
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| Source note | uspto-grants-2008_03 |
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