HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402511Generated: October 26, 2026
Diisopropylethylamine → 5-(1-(6-Chloro-5-methylpyrimidin-4-yl)piperidin-4-yl)-3-isopropyl-1,2,4-oxadiazole
https://huagongshe.com/reaction/402511
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4,6-Dichloro-5-methylpyrimidine | HCID 818860 | — |
| Reactant | 4-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidine hydrochloride | HCID 53400827 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(1-(6-Chloro-5-methylpyrimidin-4-yl)piperidin-4-yl)-3-isopropyl-1,2,4-oxadiazole | HCID 86661611 | 43% |
Reaction Steps
A solution of 4-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidine hydrochloride (2.0 gm, 0.008369 moles) and diisopropylethylamine (2.78 gm, 0.0215 moles) in dichloromethane (30 ml) was added to an ice-cooled solution of 4,6-dichloro-5-methylpyrimidine (2.1 gm, 0.001295 moles) in dichloromethane (10 ml) and the reaction was stirred at 27° C. for 2 h. The reaction mixture was diluted with dichloromethane and washed with water and brine, dried over sodium sulfate and evaporated under reduced pressure. The crude was purified by flash column chromatography (silica gel, 15% ethyl acetate in hexane) to afford the title compound as a white solid (43% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742117B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-1835680b8e5e4078a7d45ff6eb06ff2d |
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| Source note | uspto-grants-2014_06 |
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