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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892158Generated: November 1, 2026

Benzylamine → 5-Chloro-3-(1-methylethyl)-N-(phenylmethyl)pyrazolo[1,5-a]pyrimidin-7-amine

https://huagongshe.com/reaction/1892158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant5,7-Dichloro-3-(propan-2-yl)pyrazolo[1,5-a]pyrimidineHCID 21065644—
SolventEthanolHCID 702—
Product5-Chloro-3-(1-methylethyl)-N-(phenylmethyl)pyrazolo[1,5-a]pyrimidin-7-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507673B2
Source datasetuspto-grants-2013_08
ORD IDord-bfc59b9a9a51418ab06fa471f5f32279
Source noteuspto-grants-2013_08