HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036964Generated: November 1, 2026
Acetonitrile → (7-(Cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-ylethyl)benzonitrile
https://huagongshe.com/reaction/2036964
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 3-((7-Chloropyrazolo[1,5-a]pyrimidin-5-yl)methyl)benzonitrile | HCID 86654653 | — |
| Solvent | Water | HCID 962 | — |
| Product | (7-(Cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-ylethyl)benzonitrile | HCID 86654654 | 83% |
Reaction Steps
To the reaction flask, 3((7-chloropyrazolo[1,5-a]pyrimidin-5-yl)methyl)benzonitrile (400 mg, 1.5 mmol) was added along with cyclopropylamine (115 μL, 1.6 mmol), triethylamine (230 μL, 1.6 mmol), and acetonitrile (3 mL). The reaction was stirred at room temperature for 8 hours at 80° C. then cooled to room temperature, diluted with water, filtered and washed with water. The product, 3-((7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl)methyl)benzonitrile, was collected as a solid in 83% yield after drying under vacuum overnight. LCMS (M+1=290)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08575177B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-b944f62468f14de5b3e88cba04317cd4 |
|---|
| Source note | uspto-grants-2013_11 |
|---|