HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452622Generated: October 31, 2026
Isopropanol → (6-Allyl-5-chloropyrazolo[1,5-a]pyrimidin-7-yl)(4-ethoxyphenyl)amine
https://huagongshe.com/reaction/1452622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 4-Ethoxyaniline | HCID 9076 | — |
| Reactant | 6-Allyl-5,7-dichloropyrazolo[1,5-a]pyrimidine | HCID 57526845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (6-Allyl-5-chloropyrazolo[1,5-a]pyrimidin-7-yl)(4-ethoxyphenyl)amine | HCID 57526813 | 100% |
Reaction Steps
To an isopropanol (52 mL) solution containing 6-allyl-5,7-dichloropyrazolo[1,5-a]pyrimidine (5.98 g), triethylamine (12.7 mL) and phenethidine (4.30 g) were added, and this mixture was stirred at 40° C. for 5 hr. After the reaction, the solvent was distilled off. Saturated aqueous sodium hydrogen carbonate was added to the residue, and the mixture was extracted with ethyl acetate. The combined ethyl acetate layer was dried over sodium sulfate. After the sodium sulfate was filtered off, the filtrate was concentrated to obtain the title compound (8.62 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07473694B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-f59e88fd31274ea4be9ce626c26fb574 |
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| Source note | uspto-grants-2009_01 |
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