HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729458Generated: October 27, 2026
Triethylamine → 1-(5-Bromopyrimidin-2-yl)piperidin-4-ol
https://huagongshe.com/reaction/729458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | 5-Bromo-2-chloropyrimidine | HCID 606665 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(5-Bromopyrimidin-2-yl)piperidin-4-ol | HCID 4641125 | — |
Reaction Steps
A mixture of 5-bromo-2-chloropyrimidine (5 g, 25.8 mmol), piperidin-4-ol (2.88 g, 28.4 mmol) and triethylamine (5.40 mL, 38.8 mmol) in EtOH (51.7 mL) was heated at 90° C. for 0.5 h. The solvent was evaporated, the residue was diluted with 1N HCl (20 mL) and extracted with EtOAc (3×15 mL). The combined organic fractions were dried over Na2SO4 and the solvent was evaporated. The product was recrystallized from CH2Cl2/hexanes, filtered and washed with hexanes to afford the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582633B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-e75771e8633045fda7a34cfabfbb0348 |
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| Source note | uspto-grants-2009_09 |
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