HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526917Generated: November 1, 2026
Diisopropylethylamine → (R)-tert-butyl 3-((2-chloro-5-fluoropyrimidin-4-ylamino)methyl)-piperidine-1-carboxylate
https://huagongshe.com/reaction/526917
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,4-Dichloro-5-fluoropyrimidine | HCID 250705 | — |
| Reactant | tert-Butyl (3R)-3-(aminomethyl)piperidine-1-carboxylate | HCID 1502023 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-tert-butyl 3-((2-chloro-5-fluoropyrimidin-4-ylamino)methyl)-piperidine-1-carboxylate | HCID 86667415 | — |
Reaction Steps
To a solution of 2,4-dichloro-5-fluoropyrimidine (0.43 g, 2.59 mmol) and (R)-tert-butyl 3-(aminomethyl)piperidine-1-carboxylate (0.56 g, 2.59 mmol) in THF (50 mL) was added iPr2NEt (0.45 mL, 2.59 mmol). The reaction mixture was heated at 80° C. at for 8 h. The solvent was concentrated under reduced pressure and the resulting residue was purified by silica gel chromatography (5-30% EtOAc/hexanes) to afford the desired product, 11a.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345708B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-7d313eb604cc4111a1fc1c7ea12cadb4 |
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| Source note | uspto-grants-2016_05 |
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