HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878445Generated: October 30, 2026
4-Aminopyridine → HCID 62235240, compound
https://huagongshe.com/reaction/878445
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Chloropicolinic acid | HCID 20812 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 62235240 | HCID 62235240 | — |
Reaction Steps
6-Chloropicolinic acid (0.50 g, 3.17 mmol) was dissolved in thionyl chloride (5.0 mL) and stirred at 25° C. for 1 hour. The thionyl chloride was evaporated, and 4-aminopyridine (0.28 g, 2.98 mmol), triethylamine (0.415 mL, 2.98 mmol) and dichloromethane (50 mL) were added. The solution was stirred at 25° C. for 18 hours. The reaction mixture was partitioned between dichloromethane (50 mL) and saturated sodium bicarbonate solution (100 mL). The organic layer was dried (sodium sulfate) and concentrated, and the residue was purified by silica gel flash column chromatography to afford the titled compound: 1H NMR (500 MHz, methanol-D4) δ ppm 7.71 (dd, J=7.9, 0.9 Hz, 1H), 7.91-7.95 (m, 2H), 8.05 (t, J=7.8 Hz, 1H), 8.20 (dd, J=7.6, 0.6 Hz, 1H), 8.43-8.52 (m, 2H). MS (ESI) m/z=335 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987453B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-99cbe81dc5aa40c3beea78bc717371c5 |
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| Source note | uspto-grants-2015_03 |
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