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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 5,7-Dichloropyrazolo[1,5-a]pyrimidine | HCID 11074154 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-chloro-N-cyclopropylpyrazolo[1,5-a]pyrimidin-7-amine | HCID 58196606 | 70.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575177B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-7cb31d3713c34329aabcfea75bd1457f |
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| Source note | uspto-grants-2013_11 |
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