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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPiperidin-4-olHCID 79341—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
SolventEthanolHCID 702—
Product1-(5-Bromopyrimidin-2-yl)piperidin-4-olHCID 4641125—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582633B2
Source datasetuspto-grants-2009_09
ORD IDord-e75771e8633045fda7a34cfabfbb0348
Source noteuspto-grants-2009_09