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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024690Generated: October 28, 2026

Potassium Carbonate → HCID 66818499, compound

https://huagongshe.com/reaction/1024690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl N-(3-bromopropyl)carbamateHCID 4460490—
ReactantHCID 66818735HCID 66818735—
SolventDimethylformamideHCID 6228—
ProductHCID 66818499HCID 6681849988.7%

Reaction Conditions

Temperature45 °C

Reaction Steps

0.117 g (0.85 mmol) of K2CO3 and N,N-diisopropylethylamine 0.072 g (0.56 mmol) followed by 0.201 g (0.85 mmol) of (3-bromo-propyl)-carbamic acid tert-butyl ester, dissolved in 5 ml of DMF, were added to a stirred solution of 0.373 g (0.85 mmol) of 2,6-bis-(4-cyano phenoxy)-N-piperidine-4-yl nicotinamide, dissolved in 5 ml of DMF over a period of 15 min at 20° C. Reaction mixture was allowed to attain RT and heated to 45° C. for 2 h. The reaction mixture was concentrated under reduced pressure to remove the solvent. The residue was partitioned between water (150 ml) and ethyl acetate (150 ml). The organic phase was washed with 1 M Na2CO3 and saturated brine solution, and dried over sodium sulphate. The solution was concentrated and the oily residue was purified by column chromatography using hexane-ethyl acetate (10:2) to afford 0.45 g of the required product. Percentage purity (LCMS): 72.5%, (M+1)=596.2+1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722930B2
Source datasetuspto-grants-2014_05
ORD IDord-4f3070a833954303bd767c06683b71df
Source noteuspto-grants-2014_05