HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pentylamine → N-(2-Amino-5-benzyl-6-methylpyrimidine-4-yl)-N-pentylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pentylamine | HCID 8060 | — |
| Reactant | 5-Benzyl-4-chloro-6-methylpyrimidin-2-amine | HCID 820238 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(2-Amino-5-benzyl-6-methylpyrimidine-4-yl)-N-pentylamine | HCID 12043763 | 89.7% |
Reaction Steps
A mixture of 5-benzyl-4-chloro-6-methylpyrimidine-2-ylamine (500 mg, 2.14 mmol), amylamine (1.24 ml) and dioxane (4 ml) was kept at 95-100° C. for 19 hours. The reaction mixture was concentrated in vacuo, and the residue was extracted with chloroform and a saturated aqueous NaHCO3 solution. The organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (2% MeOH/CHCl3) to give the object compound (546 mg, 89.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06951866B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-9f103579a5974a6dbb5baa6adf201994 |
| Source note | uspto-grants-2005_10 |