HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21473649, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Amino-5-(chloromethyl)-2-methylpyrimidine | HCID 421245 | — |
| Reactant | HCID 21473622 | HCID 21473622 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21473649 | HCID 21473649 | 52% |
Reaction Steps
A suspension of 0.95 g (0.0050 mol) of 5-chloromethyl-2-methyl-pyrimidin-4-ylamine in 13 ml of dimethylformamide was treated with 3.5 ml (0.025 mol) of triethylamine and 1.16 g (0.010) of 4-ethyl-1,2,3,6-tetrahydropyridine and the mixture was stirred at room temperature under argon for 18 hours. The solvent was distilled off in a high vacuum. The residue was partitioned between dichloromethane/water, extracted and dried over MgSO4. After removing the solvent the residue was chromatographed on silica gel with ethyl acetate as the eluent. 0.60 g (52%) of 5-(4-ethyl-3,6-dihydro-2H-pyridin-1-ylmethyl)-2-methyl-pyrimidin-4-ylamine were obtained as a beige solid; m.p. 75°-76°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688798 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-e1c4fa5adb774828a108934667006266 |
| Source note | uspto-grants-1997_11 |