HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574692Generated: October 27, 2026
2-(3-(5-methyl-1H-imidazol-1-yl)propyl)isoindoline-1,3-dione → 3-(5-methyl-1H-imidazol-1-yl)propan-1-amine
https://huagongshe.com/reaction/574692
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(3-(5-methyl-1H-imidazol-1-yl)propyl)isoindoline-1,3-dione | HCID 18722266 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(5-methyl-1H-imidazol-1-yl)propan-1-amine | HCID 19429483 | — |
Reaction Steps
2-(3-(5-methyl-1H-imidazol-1-yl)propyl)isoindoline-1,3-dione (i.e. 8.92 mmol, 1 eq.) and hydzine monohydrate (17.84 mmol, 2eq.) were dissolved in dry EtOH (50 mL). The mixture was kept under reflux over night, then mixture was concentrated down to a volume of 25 mL. After that hydrochloric acid (conc., 55 mL) was added and the mixture was heated up to 50° C. for and kept at this temperature for 30 min. The formed precipitate was filtered off. The filtrate was cooled down to 0° C. and solid NaOH was added until a final pH-value of 10-12 is reached. The aqueous solution was extracted by means of CHCl3 (3×50 mL). The combined organic layers were dried over Na2SO4, filtered and the solvent was removed. The product was purified by means of flash-chromatography using silica gel and a CHCl3/MeOH-gradient.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09034907B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-977925ce00794f0ea18550834da21e1f |
|---|
| Source note | uspto-grants-2015_05 |
|---|