HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852023Generated: October 26, 2026
Potassium Fluoride → 3-{3-Cyano-6-[(2,2-dimethyl-propyl)-amino]-5-fluoro-pyridin-2-ylamino}-N-methoxy-4-methyl-benzamide
https://huagongshe.com/reaction/852023
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 3-Amino-N-methoxy-4-methylbenzamide | HCID 20767000 | — |
| Reactant | 2-Chloro-6-[(2,2-dimethyl-propyl)-amino]-5-fluoro-nicotinonitrile | HCID 86588798 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-{3-Cyano-6-[(2,2-dimethyl-propyl)-amino]-5-fluoro-pyridin-2-ylamino}-N-methoxy-4-methyl-benzamide | HCID 10134671 | 1% |
Reaction Steps
A mixture of 2-chloro-6-[(2,2-dimethyl-propyl)-amino]-5-fluoro-nicotinonitrile (150 mg, 0.62 mmol), 3-amino-N-methoxy-4-methyl-benzamide (150 mg, 0.83 mmol) and potassium fluoride (30 mg, 0.51 mmol) in DMSO (1 mL) was heated to 150° C. overnight. The reaction mixture was allowed to cool to room temp and then partitioned between water and ethyl acetate. The organic layer was dried (sodium sulfate) and concentrated under reduced pressure. The product (2.5 mg, 1%) was obtained after purification by silica gel chromatography with 30% EtOAc in hexane as eluent. C20H24FN5O2 MS m/e=386 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07253174B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-d7d86ab8b68c46d4b050f45baeb8f0a4 |
|---|
| Source note | uspto-grants-2007_08 |
|---|