HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520733Generated: October 30, 2026
Tert-Butylamine → 2-Pyridinecarboxamide, 5-bromo-N-(1,1-dimethylethyl)-
https://huagongshe.com/reaction/520733
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Bromopyridine-2-carboxylic acid | HCID 608544 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Pyridinecarboxamide, 5-bromo-N-(1,1-dimethylethyl)- | HCID 10999696 | 92.3% |
Reaction Steps
5-Bromopicolinic acid (200 mg, 0.99 mmol) was dissolved in dioxane (2 ml) and Hunig's Base (520 μl, 2.97 mmol, 3 equiv.), TBTU (350 mg, 1.09 mmol, 1.1 equiv.) and tert-butyl amine (124 μl, 1.19 mmol, 1.2 equiv.) were added at room temperature. The mixture was stirred for 16 hours at room temperature. The reaction mixture was evaporated and extracted saturated NaHCO3 solution and two times with a small volume of dichloromethane. The crude product was purified by flash chromatography by directly loading the dichloromethane layers onto a silica gel column and eluting with an ethyl acetate:heptane gradient 0:100 to 50:50. The desired 5-bromo-pyridine-2-carboxylic acid tert-butylamide (235 mg, 92% yield) was obtained as a colorless oil, MS: m/e=257.0/259.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328070B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-73af5e4c2f7945d5ade73abfad7d2108 |
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| Source note | uspto-grants-2016_05 |
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