HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226446Generated: October 30, 2026
Ammonium formate → ethyl 6-(2,3-dihydro-1H-inden-2-ylamino)nicotinate
https://huagongshe.com/reaction/226446
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | ethyl 5-chloro-6-(2,3-dihydro-1H-inden-2-ylamino)nicotinate | HCID 68960178 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 6-(2,3-dihydro-1H-inden-2-ylamino)nicotinate | HCID 68966760 | 29.5% |
Reaction Steps
To a mixture of ethyl 5-chloro-6-(2,3-dihydro-1H-inden-2-ylamino)nicotinate (395 mg) and ammonium formate (472 mg) in ethanol (10 mL) was added 10% palladium on carbon (40 mg), and the mixture was stirred at 100° C. for 10 hours. The catalyst in the reaction mixture was removed by filtration. The solvent was evaporated in vacuo. The residual solid was collected with hexane and ethyl acetate (2/1 v/v) to give ethyl 6-(2,3-dihydro-1H-inden-2-ylamino)nicotinate (104 mg). The mother liquid was concentrated in vacuo, and the residue was purified by preparative thin layer column chromatography (hexane/ethyl acetate=2/1) to give ethyl 6-(2,3-dihydro-1H-inden-2-ylamino)nicotinate (209 mg) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557127B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-de2e8522374b4f8caa1df0813c65de00 |
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| Source note | uspto-grants-2009_07 |
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