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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,5-Trimethyloxazole | HCID 30215 | — |
| Reactant | 4-(3-Aminopropyl)piperidine-1-carbaldehyde | HCID 20239778 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-[3-(2,4,5-trimethyl-1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde | HCID 20239777 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04537969 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-177110fcdaef4a71a576236c57916079 |
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| Source note | uspto-grants-1985_08 |
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