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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-(5-methyl-1H-imidazol-1-yl)propyl)isoindoline-1,3-dioneHCID 18722266—
SolventEthanolHCID 702—
Product3-(5-methyl-1H-imidazol-1-yl)propan-1-amineHCID 19429483—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034907B2
Source datasetuspto-grants-2015_05
ORD IDord-977925ce00794f0ea18550834da21e1f
Source noteuspto-grants-2015_05