HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutylamine → Isobutyl-(8-propyl-[1,2,4]triazolo[1,5-c]pyrimidin-7-ylmethyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Bromomethyl-8-propyl-[1,2,4]triazolo[1,5-c]pyrimidine | HCID 57503311 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Isobutyl-(8-propyl-[1,2,4]triazolo[1,5-c]pyrimidin-7-ylmethyl)-amine | HCID 58661548 | — |
Reaction Steps
To a solution of 7-bromomethyl-8-propyl-[1,2,4]triazolo[1,5-c]pyrimidine (16.58 mmol) in CH3CN (30 ml) is added K2CO3 (9.15 g, 66.3 mmol), isobutylamine (6.6 ml, 66.3 mmol) and the mixture is stirred at room temperature overnight. The solvent is removed in vacuo and to the residue is added water (60 ml) and EtOAc (60 ml). The layers are separated and the organic layer is washed with brine (20 ml) and dried (Na2SO4). Evaporation of the solvent provides a light yellow oil, which is used in next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351826B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-d18e2a2c015e447f99bc6b735389ae70 |
| Source note | uspto-grants-2008_04 |