HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Amino-N-(5-(4-chloro-phenoxy)-thiophen-2-ylmethyl)-nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Aminonicotinic acid | HCID 72930 | — |
| Reactant | Benzotriazol-1-yltris(dimethylamino)phosphonium hexafluorophosphate | HCID 10938826 | — |
| Reactant | C-(5-(4-chloro-phenoxy)-thiophen-2-yl)-methylamine | HCID 23130383 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | 2-Amino-N-(5-(4-chloro-phenoxy)-thiophen-2-ylmethyl)-nicotinamide | HCID 23130691 | 24.9% |
Reaction Steps
A solution of 2-amino-nicotinic acid (21 mg, 0.15 mmol), C-(5-(4-chloro-phenoxy)-thiophen-2-yl)-methylamine described in Preparation Example 157 (36 mg, 0.15 mmol), benzotriazol-1-yl-tris(dimethylamino)phosphonium hexafluorophosphate (86 mg, 0.195 mmol) and triethylamine (0.065 mL, 0.45 mmol) in dimethylsulfoxide (1 mL) was stirred under nitrogen atmosphere for 17 hours at room temperature. This reaction solution was purified by reverse phase high performance liquid chromatography (acetonitrile-water mobile phase (containing 0.1% trifluoroacetic acid) was used), and trifluoroacetic acid salt of the title compound (17.7 mg, 0.037 mmol, 24.9%) was obtained as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932272B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-83f7496b09fc48f5ae03c07e2e50694f |
| Source note | uspto-grants-2011_04 |