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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383373Generated: October 31, 2026

Diisopropylethylamine → 2-[2-(4-{2-[4-({3-[(R)-cyclohexyl(hydroxy)phenylmethyl]-1H-1,2,4-triazol-1-yl}methyl)piperdin-1-yl]ethyl}phenyl)ethyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/2383373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-{2-[4-(2-Bromo-ethyl)-phenyl]-ethyl}-isoindole-1,3-dioneHCID 59145947—
Reactantcyclohexyl(phenyl)[1-(piperidin-4-ylmethyl)-1H-1,2,4-triazol-3-yl]methanolHCID 59145970—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-[2-(4-{2-[4-({3-[(R)-cyclohexyl(hydroxy)phenylmethyl]-1H-1,2,4-triazol-1-yl}methyl)piperdin-1-yl]ethyl}phenyl)ethyl]-1H-isoindole-1,3(2H)-dioneHCID 5914596274%

Reaction Conditions

Temperature90 °C

Reaction Steps

Cyclohexyl-phenyl-(1-piperidin-4-ylmethyl-1H-[1,2,4]triazol-3-yl)-methanol (Preparation 4, 0.40 g, 1.13 mmol) and 2-{2-[4-(2-Bromo-ethyl)-phenyl]-ethyl}-isoindole-1,3-dione (Preparation 11, 0.404 g, 1.13 mmol) and diisopropylethylamine (0.59 ml, 3.38 mmol) were dissolved in methyl ethyl ketone (8 mL). After stirring at 90° C. for 24 hours the reaction was allowed to cool slowly to room temperature. Crystallisation occured and the resulting solid was collected by filtration and dried in vacuo to yield the title compound as a cream coloured solid, in 74% yield, 0.532 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263623B2
Source datasetuspto-grants-2012_09
ORD IDord-86bf0295a7ec4e3f8f1228b37216da3f
Source noteuspto-grants-2012_09