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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619447Generated: October 31, 2026

4-((4-(2,2-Dimethyl-1,3-dioxan-5-yl)phenoxy)methyl)-2-(1-(pyrimidin-2-yl)piperidin-4-yl)thiazole → 2-(4-((2-(1-(Pyrimidin-2-yl)piperidin-4-yl)thiazol-4-yl)methoxy)phenyl)propane-1,3-diol

https://huagongshe.com/reaction/1619447

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((4-(2,2-Dimethyl-1,3-dioxan-5-yl)phenoxy)methyl)-2-(1-(pyrimidin-2-yl)piperidin-4-yl)thiazoleHCID 67510151—
SolventAcetoneHCID 180—
SolventHydrochloric AcidHCID 313—
Product2-(4-((2-(1-(Pyrimidin-2-yl)piperidin-4-yl)thiazol-4-yl)methoxy)phenyl)propane-1,3-diolHCID 67515956117.2%

Reaction Conditions

Temperature27 °C

Reaction Steps

To a solution of 4-((4-(2,2-dimethyl-1,3-dioxan-5-yl)phenoxy)methyl)-2-(1-(pyrimidin-2-yl)piperidin-4-yl)thiazole (500 mg, 0.0010 moles) in acetone (20 ml), conc. HCl (2 ml) was added portion-wise and the reaction mixture was stirred for 12 hours at 27° C. The reaction mixture was concentrated and the residue was dissolved in ethyl acetate. The organic layer was successively washed with water & brine, dried over sodium sulfate and evaporated under reduced pressure to yield 500 mg product as white solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772302B2
Source datasetuspto-grants-2014_07
ORD IDord-0b867fc9a9834705914604ef64f1fc01
Source noteuspto-grants-2014_07