HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054107Generated: October 26, 2026
p-Fluoronitrobenzene → 3-methyl-N-(4-nitrophenyl)pyrid-2-amine
https://huagongshe.com/reaction/2054107
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Amino-3-methylpyridine | HCID 15347 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 3-methyl-N-(4-nitrophenyl)pyrid-2-amine | HCID 23104477 | 36.9% |
Reaction Steps
0.3 g of 4-fluoronitrobenzene, 0.46 g of 2-amino-3-methylpyridine, and 0.353 g of K2CO3 were added to a solution of 2.5 ml of N-methylpyrrolidinone. The reaction medium was heated at 60° C. for 1 hour and 0.286 g of potassium tert-butoxide was then added. Heating was then continued for 6 hours and, after cooling to room temperature, the reaction medium was then poured into a water and ice mixture. The yellow precipitate formed was filtered off, reslurried in water and then dried over P2O5. 0.18 g of 3-methyl-N-(4-nitrophenyl)pyrid-2-amine (7) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07329288B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-1d63e4b2be784c96873ad1d1a9773058 |
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| Source note | uspto-grants-2008_02 |
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