HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 3-[3-(4-Amino-[1,3,5]triazin-2-yl)-pyridin-2-ylamino]-N-(4-phenoxy-phenyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4-(2-chloropyridin-3-yl)-N-(3,4,5-trimethoxyphenyl)-1,3,5-triazin-2-amine | HCID 16109005 | — |
| Reactant | 3-Amino-N-(4-phenoxyphenyl)benzamide | HCID 22560095 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-[3-(4-Amino-[1,3,5]triazin-2-yl)-pyridin-2-ylamino]-N-(4-phenoxy-phenyl)benzamide | HCID 10162549 | — |
Reaction Steps
[4-(2-Chloro-pyridin-3-yl)-[1,3,5]triazin-2-yl]-(3,4,5-trimethoxy-phenyl)amine (Example 2, Step 4) (247 mg, 1.08 mmol) was suspended in a 2 M solution of NH3 in IpOH (3 ml)(Aldrich), and the reaction mixture was stirred overnight in a sealed tube. Concentration, trituration in a small amount of MeOH, and filtration provided a white solid. A portion of this material (97 mg, 0.47 mmol) was mixed with 3-amino-N-(4-phenoxyphenyl)benzamide (320 mg, 0.96 mmol) and DMSO (250 ml), and stirred overnight at 90° C. The dark residue was diluted with IpOH, sonicated, triturated, and then concentrated. Upon dilution with IpOH, a light green solid was isolated by filtration. MS m/z=476.5. [M+H]+. Calc'd for C27H21N7O2: 475.18.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06864255B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-81e7ecd6542446169c6890c6ef5cc728 |
| Source note | uspto-grants-2005_03 |