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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850793Generated: October 30, 2026

Diisopropylethylamine → HCID 86711210, compound

https://huagongshe.com/reaction/1850793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-bromo [1,2,4]triazolo[1,5-a]pyrimidineHCID 77230929—
Reactant2-((1S,2R)-2-(piperidin-4-yl)cyclopropyl)ethanolHCID 86711178—
SolventEthanolHCID 702—
ProductHCID 86711210HCID 86711210—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a mixture of 2-((1S,2R)-2-(piperidin-4-yl)cyclopropyl)ethanol (Intermediate 11; 70 mg, 0.4 mmol) and 2-bromo[1,2,4]triazolo[1,5-a]pyrimidine (9 mg, 0.496 mmol) in ethanol (2 mL) was added DIEA (0.22 mL, 1.21 mmol) and the resulting mixture heated via microwave to 120° C. for 1 hr. HPLC of the reaction mixture proved the reaction was complete with the absence of Intermediate 11. The mixture was filtered (glass wool filter paper, Whatman 1821 110), and washed with ethanol. The filtrate was concentrated to dryness under reduced pressure and the resulting residue purified via preparative TLC plates (2×1000 μM silica gel) eluting with 50% ethyl acetate in hexane. The product was removed from the silica gel by extracting with ethyl acetate and the solvent was removed under reduced pressure to afford the title compound as an off-white solid. MS (Multimode) m/z 288 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957062B2
Source datasetuspto-grants-2015_02
ORD IDord-4f639b887703481c9d16189af27e5ef4
Source noteuspto-grants-2015_02