HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201707Generated: October 29, 2026
Sodium Bicarbonate → N-(2-amino-5-(pyridin-3-yl)phenyl)pyrrolidine-1-carboxamide
https://huagongshe.com/reaction/2201707
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Pyridinylboronic acid | HCID 2734378 | — |
| Reactant | N-(2-amino-5-bromophenyl)pyrrolidine-1-carboxamide | HCID 86712537 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-amino-5-(pyridin-3-yl)phenyl)pyrrolidine-1-carboxamide | HCID 71466381 | 68.9% |
Reaction Steps
To a solution of N-(2-amino-5-bromophenyl)pyrrolidine-1-carboxamide (0.26 g, 0.72 mmol) in THF (10 mL) and water (5 mL) were added pyridin-3-ylboronic acid (0.13 g, 1.07 mmol, 1.5 equiv.), sodium bicarbonate (0.11 g, 1.07 mmol, 1.5 equiv.) and palladium(0) (0.08 g, 0.07 mmol, 0.1 equiv.). The reaction mass was stirred at 90° C. for sixteen hours. The reaction crude was filtered on a celite bed and diluted in ethyl acetate. The organic layers were washed with water and brine then dried over Na2SO4 and concentrated. The residue was purified by column chromatography on eluting ethyl acetate and hexane to allow N-(2-amino-5-(pyridin-3-yl)phenyl)pyrrolidine-1-carboxamide (0.14 g, 63% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365498B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-2f7fc84e83604e9897f456091a5c05e2 |
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| Source note | uspto-grants-2016_06 |
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