HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-methyl-5-(7-phenyl-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-pyrimidin-4-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-Phenyl-1,2,3,4-tetrahydroisoquinoline | HCID 32400 | — |
| Reactant | 4-Amino-5-(chloromethyl)-2-methylpyrimidine | HCID 421245 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-methyl-5-(7-phenyl-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-pyrimidin-4-ylamine | HCID 21473699 | 76% |
Reaction Steps
A suspension of 0.17 g (0.00088 mol) of 5-chloromethyl-2-methyl-pyrimidin-4-ylamine in 10 ml of dimethylformamide was treated with 0.30 ml (0.0021 mol) of triethylamine and 0.184 g (0.00088 mol) of 7-phenyl-1,2,3,4-tetrahydro-isoquinoline 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 over silica gel with ethyl acetate as the eluent. 0.22 g (76%) of 2-methyl-5-(7-phenyl-3,4-dihydro-1H-isoquinolin-2-ylmethyl)-pyrimidin-4-ylamine was obtained as a light yellowish solid; m.p. 147°-149°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688798 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-ccd32a52a53c4457a4e475fcb3e7686e |
| Source note | uspto-grants-1997_11 |