HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82671Generated: October 26, 2026
Water → N2-[4-(benzyloxy)phenyl]-5-fluoropyridine-2,3-diamine
https://huagongshe.com/reaction/82671
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Benzyloxyaniline | HCID 22860 | — |
| Reactant | 2-Chloro-5-fluoro-3-nitropyridine | HCID 10773626 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N2-[4-(benzyloxy)phenyl]-5-fluoropyridine-2,3-diamine | HCID 58577701 | 24.3% |
Reaction Steps
A mixture of 4-(benzyloxy)aniline (2.26 g), 2-chloro-5-fluoro-3-nitropyridine (2 g) and K2CO3 (3.13 g) in DMF (20 mL) was stirred at 120° C. for 5 h, treated with water, and extracted with AcOEt. The organic layer was dried over MgSO4 and concentrated in vacuo. The residue was suspended in IPE and collected by filtration. The solid obtained above was dissolved in EtOH (20 mL), and Pt/C (2 g) was added. Under H2 atmosphere, the mixture was stirred for 1 h, filtered and evaporated. The residue was chromatographed on silica gel eluting with Hexane/AcOEt to give the title compound (0.85 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846713B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-0378987afca642479291af01bdd7ec35 |
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| Source note | uspto-grants-2014_09 |
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