HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Aminopyridine → 4-Methyl-n-(2,2,2-trifluoro-1-{[(3-pyridinylamino)carbothioyl]amino}ethyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Aminopyridine | HCID 10009 | — |
| Reactant | 4-methyl-N-(2,2,2-trifluoro-1-isothiocyanatoethyl)benzamide | HCID 12150324 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-Methyl-n-(2,2,2-trifluoro-1-{[(3-pyridinylamino)carbothioyl]amino}ethyl)benzamide | HCID 9907285 | — |
Reaction Steps
A solution of 3-aminopyridine (145 mg, 1.54 mmol) in benzene (8 mL) at ambient temperature was treated with a solution of Example 1C (500 mg, 1.54 mmol) in benzene (1.5 mL). The reaction mixture was stirred for 1.5 hours, then concentrated to a nominal volume. The white solids which precipitated from solution were collected by filtration and were washed with diethyl ether. Recrystallization from 25% ethyl acetate/hexanes provided the desired product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06645968B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-6e80e82d492d4cf3961678cbba023c38 |
| Source note | uspto-grants-2003_11 |