HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890501Generated: October 31, 2026
Triethylamine → 2-(2-Acetylaminopyrimidin-4-ylmethylthio)-N-(3,5-dimethylphenyl)pyridine-3-carboxamide
https://huagongshe.com/reaction/1890501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-(3,5-Dimethylphenyl)-2-thioxo-1,2-dihydropyridine-3-carboxamide | HCID 23151038 | — |
| Reactant | 2-Acetylamino-4-chloromethylpyrimidine | HCID 45119260 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Acetylaminopyrimidin-4-ylmethylthio)-N-(3,5-dimethylphenyl)pyridine-3-carboxamide | HCID 11964855 | 52% |
Reaction Steps
Triethylamine (45 mL, 0.32 mmol) was added to a solution of N-(3,5-dimethylphenyl)-2-thioxo-1,2-dihydropyridine-3-carboxamide (28 mg, 0.11 mmol, Reference Compound No. 13-1) and 2-acetylamino-4-(chloromethyl)pyrimidine (18 mg, 0.10 mmol, Reference Compound No. 11-1) in anhydrous N,N-dimethylformamide (1.0 mL) at room temperature, and the mixture was stirred for 16 hours. Ethyl acetate (30 mL) was added thereto, then the whole was washed with saturated aqueous sodium hydrogencarbonate solution (30 mL) and brine (30 mL), and the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and then the precipitated solid was filtered off with diethyl ether and washed. The solid was dried at 50° C. under reduced pressure to give 21 mg of the target compound as a light orange solid (Yield: 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08507485B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-3db15bbec82f4bf091a291be43c11b1c |
|---|
| Source note | uspto-grants-2013_08 |
|---|