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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036991Generated: November 4, 2026

Triethylamine → 5-chloro-N-cyclopropylpyrazolo[1,5-a]pyrimidin-7-amine

https://huagongshe.com/reaction/2036991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclopropylamineHCID 69828—
Reactant5,7-Dichloropyrazolo[1,5-a]pyrimidineHCID 11074154—
SolventAcetonitrileHCID 6342—
Product5-chloro-N-cyclopropylpyrazolo[1,5-a]pyrimidin-7-amineHCID 5819660670.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 5,7-dichloropyrazolo[1,5-a]pyrimidine (200 mg, 1.06 mmol) in acetonitrile was added Et3N (148 μl, 1.06 mmol) and cyclopropylamine (75 μl, 1.06 mmol). The reaction was heated at 80° C. overnight. The mixture was concentrated under reduced pressure, dissolved in dichloromethane, and washed with water. The resulting organic layer was dried over Na2SO4 and concentrated under reduced pressure to afford 156 mg of 5-chloro-N-cyclopropylpyrazolo[1,5-a]pyrimidin-7-amine (70% yield). LCMS (M+1=209)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575177B2
Source datasetuspto-grants-2013_11
ORD IDord-7cb31d3713c34329aabcfea75bd1457f
Source noteuspto-grants-2013_11