HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631394Generated: November 3, 2026
Diisopropylethylamine → HCID 66848002, compound
https://huagongshe.com/reaction/1631394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 5-chloropyrazolo(1,5-a)pyrimidine-3-carboxylate | HCID 58063474 | — |
| Reactant | HCID 66848129 | HCID 66848129 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 66848002 | HCID 66848002 | 14% |
Reaction Steps
A mixture of ((2S,5R)-5-(5-fluoropyridin-3-yl)pyrrolidin-2-yl)methanol (0.910 g, 4.64 mmol), ethyl 5-chloropyrazolo[1,5-a]pyrimidine-3-carboxylate (Preparation B, 1.05 g, 4.64 mmol) and DIEA (1.10 mL, 6.00 mmol) in isopropyl alcohol (1.0 mL) was heated at 90° C. for 16 hours. The reaction mixture was concentrated and the residue was purified by reverse phase column chromatography (0-50% acetonitrile/water) followed by normal phase column chromatography (2-5% MeOH/DCM) to afford ethyl 5-((2R,5S)-2-(5-fluoropyridin-3-yl)-5-(hydroxymethyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate (0.250 g, 14% yield) as a viscous, clear oil. MS (apci) m/z=386.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791123B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-ebb50b022ffc468fb9973b57d677e5ca |
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| Source note | uspto-grants-2014_07 |
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