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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429547Generated: November 1, 2026

Potassium Carbonate → 6-Bromo-2-((1-(5-propylpyrimidin-2-yl)piperidin-4-yl)methyl)benzo[d]oxazole

https://huagongshe.com/reaction/1429547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-propylpyrimidineHCID 2735784—
Reactant6-Bromo-2-(piperidin-4-ylmethyl)benzo[d]oxazoleHCID 67466284—
SolventDimethylformamideHCID 6228—
Product6-Bromo-2-((1-(5-propylpyrimidin-2-yl)piperidin-4-yl)methyl)benzo[d]oxazoleHCID 6746494483.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 6-bromo-2-(piperidin-4-ylmethyl)benzo[d]oxazole (0.13 g, 0.440 mmol), 2-chloro-5-propylpyrimidine (0.083 g, 0.529 mmol), and K2CO3 (0.122 g, 0.881 mmol) in DMF (4.4 mL) was heated in 90° C. oil bath for 12 h. It was cooled to rt, quenched with H2O (5 mL), and extracted with EtOAc-Et2O (3×4 mL, 1:1 v/v). The combined organic layers were washed with H2O (3×4 mL) and brine (4 mL). The solvent was evaporated to afford crude product, which was purified by column chromatography (silica gel, hexanes-EtOAc gradient 0-60% EtOAc) to afford the desired product as a colorless oil (153 mg, 83% yield). 1H NMR (500 MHz, CDCl3) δ 8.14 (s, 2H), 7.66 (d, J=1.8 Hz, 1H), 7.53 (d, J=8.4 Hz, 1H), 7.43 (dd, J=8.4, 1.8 Hz, 1H), 4.73 (d, J=13.4 Hz, 2H), 3.04-2.77 (m, 4H), 2.48-2.32 (m, 2H), 2.24 (s, 1H), 1.85 (d, J=12.6 Hz, 2H), 1.67-1.49 (m, 2H), 1.37 (ddd, J=25.0, 12.4, 4.2 Hz, 2H), 0.92 (t, J=7.3 Hz, 3H). LCMS (m/z)=415 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940716B2
Source datasetuspto-grants-2015_01
ORD IDord-df2e764ca28f49ad8250314bd87bd8ff
Source noteuspto-grants-2015_01