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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485816Generated: October 25, 2026

2,4,5-Trimethyloxazole → 4-[3-(2,4,5-trimethyl-1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde

https://huagongshe.com/reaction/485816

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,5-TrimethyloxazoleHCID 30215—
Reactant4-(3-Aminopropyl)piperidine-1-carbaldehydeHCID 20239778—
SolventAcetic AcidHCID 176—
Product4-[3-(2,4,5-trimethyl-1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehydeHCID 2023977750%

Reaction Conditions

Temperature145 °C

Reaction Steps

A mixture of trimethyloxazole (10.18 g, 0.091M), 4[3-aminopropyl]-1-piperidinecarboxaldehyde and acetic acid (0.16 g) were heated at 145° C. for 6 hrs. After the reaction, the excess of trimethyl oxazole was removed at reduced pressure and the residue was purified on silica gel column eluted with 4 to 10% of methanol by volume in CHCl3 to yield 4-[3-(2,4,5-trimethyl-1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde as an oil (3.3 g, 50% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04537969
Source datasetuspto-grants-1985_08
ORD IDord-177110fcdaef4a71a576236c57916079
Source noteuspto-grants-1985_08