HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368415Generated: October 31, 2026
N-methyl-2-pyrrolidone → 2-Amino-3,5-difluoro-6-(p-methoxybenzylamino)-4-methylpyridine
https://huagongshe.com/reaction/368415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | 3,5,6-Trifluoro-4-methylpyridin-2-amine | HCID 12508092 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Amino-3,5-difluoro-6-(p-methoxybenzylamino)-4-methylpyridine | HCID 22121271 | 38.7% |
Reaction Steps
To 3 ml of N-methylpyrrolidone were added 1.35 g of 2-amino-3,5,6-trifluoro-4-methylpyridine together with 3.0 g of p-methoxybenzylamine, and the mixture was stirred under nitrogen atmosphere at 140° C. for 18 hours and allowed to cool. After adding 30 ml of chloroform, the mixture was washed three times with 300 ml of distilled water. The chloroform layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to chromatography (silica gel, 20 g; eluent: chloroform:n-hexane, 1:1, and then, chloroform) to obtain 0.90 g of the title compound as a pale yellow crude oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133284 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-27aacc9ee6fd40bbb7e45e1520283585 |
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| Source note | uspto-grants-2000_10 |
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