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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673756Generated: October 26, 2026

Diisopropyl Ether → 3-(4-Isopropoxyphenyl)-2-methyl-5-{[2'-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-6-propylpyrimidin-4(3h)-one potassium salt

https://huagongshe.com/reaction/1673756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
ReactantHCID 53628223HCID 53628223—
Reactant3-(4-isopropoxyphenyl)-2-methyl-5-{[2'-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-6-propylpyrimidin-4(3H)-oneHCID 135845010—
SolventEthanolHCID 702—
Product3-(4-Isopropoxyphenyl)-2-methyl-5-{[2'-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-6-propylpyrimidin-4(3h)-one potassium saltHCID 13633103156%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 3-(4-isopropoxyphenyl)-2-methyl-5-{[2′-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-6-propylpyrimidin-4(3H)-one (200 g), ethanol (200 mL), and diisopropyl ether (400 mL) was added potassium 2-ethyl hexanoate and the mixture was stirred at 60° C. for 1 hr. To the mixture was added diisopropyl ether (1000 mL) dropwise. The mixture was stirred at reflux temperature for 24 hr, followed by being cooled to room temperature. The obtained precipitate was collected, washed with diisopropyl ether, and dried under reduced pressure at 60° C. for 1 hr to give the title compound (120 g, 56%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998968B2
Source datasetuspto-grants-2011_08
ORD IDord-ec2f6da642854e5fab3d3e441398c084
Source noteuspto-grants-2011_08