HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335329Generated: October 25, 2026
Methyl 3-amino-4-fluorobenzoate → 3-Amino-N-(2-(2,6-cis-dimethylpiperidin-1-yl)ethyl)-4-fluorobenzamide
https://huagongshe.com/reaction/335329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 3-amino-4-fluorobenzoate | HCID 12541234 | — |
| Reactant | 2-(2,6-cis-Dimethylpiperidin-1-yl)ethanaminium chloride | HCID 86695686 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Amino-N-(2-(2,6-cis-dimethylpiperidin-1-yl)ethyl)-4-fluorobenzamide | HCID 86695685 | — |
Reaction Steps
A mixture comprising 2-(2,6-cis-dimethylpiperidin-1-yl)ethanaminium chloride (4 g, 20.75 mmol) and methyl 3-amino-4-fluorobenzoate (3.51 g, 20.75 mmol) in THF (50 ml) was treated with TBD (2.89 g, 20.75 mmol) and stirred at 80° C. for 16 hrs. A further portion of methyl 3-amino-4-fluoro benzoate (1 g) and TBD (0.5 g) were added and heating continued for 24 hrs. The resulting mixture was partitioned between ethyl acetate and aqueous sodium bicarbonate. The mixture was extracted once with ethyl acetate and once with chloroform. The combined organic layers were dried (MgSO4), filtered and evaporated to dryness. Purification of the residue by chromatography on silica eluting with 0-20% MeOH in DCM afforded the title compound;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883819B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-d178de8669854224be446ae2ef0dd305 |
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| Source note | uspto-grants-2014_11 |
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