HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycine → N-(5-methoxypyrimidin-2-yl)hexanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycine | HCID 750 | — |
| Reactant | Hexanoyl chloride | HCID 67340 | — |
| Reactant | 2-Amino-5-methoxypyrimidine | HCID 2305244 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(5-methoxypyrimidin-2-yl)hexanamide | HCID 57346488 | 84% |
Reaction Steps
5-Methoxypyrimidin-2-amine (12.3 g, 98.3 mmol) was dissolved in pyridine (123 mL), the solution was added with hexanoyl chloride (14.5 g, 108 mmol) on an ice bath, and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was added with 1 M aqueous glycine (98.3 mL) at 0° C., and the mixture was stirred for 1 hour, and then extracted with chloroform. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure, and the resulting residue was azeotroped with toluene. The resulting residue was recrystallized from chloroform-hexane to obtain N-(5-methoxypyrimidin-2-yl)hexanamide (18.4 g, 84%) as colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08012989B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-2e13672ab3d3491db9e195c671fd507e |
| Source note | uspto-grants-2011_09 |