Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Amino-2-(2-furyl)-7-piperazinyl[1,2,4]triazolo[1,5-c]-pyrimidine hydrochloride | HCID 22002432 | — |
| Product | Acetate hexane | HCID 22139250 | — |
Reaction Steps
In 10 ml of DMF, 400 mg (1.04 mmol) of Compound 43 obtained in Example 43 was dissolved, and 0.51 ml (3.6 mmol) of 2-phenylethyl bromide and 1 ml of triethylamine were added thereto, followed by stirring at 60° C. for 2 hours. The reaction mixture was extracted by adding chloroform and water, and the organic phase was dried over anhydrous magnesium sulfate. After evaporation of the solvent under reduced pressure, the residue was purified by silica gel column chromatography [chloroform-methanol (97:3)] and recrystallized from ethyl. acetate-hexane to give 369 mg (yield: 95%) of Compound 46 as light gray powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06222035B1 |
|---|
| Source dataset | uspto-grants-2001_04 |
|---|
| ORD ID | ord-f8d96c12c1364e309b040b8fbf6bae6f |
|---|
| Source note | uspto-grants-2001_04 |
|---|