HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368492Generated: October 30, 2026
Benzene → 3,5-Difluoro-2-isopropylamino-6-(p-methoxybenzylamino)pyridine
https://huagongshe.com/reaction/368492
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | 2,3,5-Trifluoro-6-isopropylaminopyridine | HCID 22121278 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3,5-Difluoro-2-isopropylamino-6-(p-methoxybenzylamino)pyridine | HCID 22121218 | — |
Reaction Steps
To 4.1 g of N-methylpyrrolidone were added all amount of the 2,3,5-trifluoro-6-isopropylaminopyridine as described above together with 3.1 g of p-methoxybenzylamine, and the mixture was stirred at 150° C. for 15 hours and allowed to cool. After adding 50 ml of the mixed solution of benzene and n-hexane (1:1, v/v), the solution was washed twice with 400 ml of distilled water. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 3.9 g of the title compound as a brown 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-f6d1e0f656fb4526b9a779583f1e3f56 |
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| Source note | uspto-grants-2000_10 |
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