HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 5-Chloro-3-(1-methylethyl)-N-(phenylmethyl)pyrazolo[1,5-a]pyrimidin-7-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 5,7-Dichloro-3-(propan-2-yl)pyrazolo[1,5-a]pyrimidine | HCID 21065644 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Chloro-3-(1-methylethyl)-N-(phenylmethyl)pyrazolo[1,5-a]pyrimidin-7-amine | HCID 25123362 | — |
Reaction Steps
5,7-dichloro-3-isopropylpyrazolo[1,5-α]pyrimidine (500 mg, 2.17 mmol) and benzyl amine (0.52 mL, 4.78 mmol) in EtOH (20 mL) were refluxed for about 3 hours. The reaction mixture was then cooled to ambient temperature and concentrated in vacuo. The remaining residue was purified by flash chromatography on silica (methanol/ethyl acetate) to yield N-benzyl-5-chloro-3-isopropylpyrazolo[1,5-α]pyrimidin-7-amine as a white solid in analytically pure form (630 mg, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507673B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-bfc59b9a9a51418ab06fa471f5f32279 |
| Source note | uspto-grants-2013_08 |