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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393690Generated: October 25, 2026

Isoindoline → 3-Amino-1-(1,3-dihydroisoindol-2-yl)-3-methylbutan-1-one

https://huagongshe.com/reaction/1393690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoindolineHCID 422478—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Amino-3-methylbutanoic acidHCID 2760933—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
Product3-Amino-1-(1,3-dihydroisoindol-2-yl)-3-methylbutan-1-oneHCID 1153587860.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

2,3-Dihydro-1H-isoindole (543 mg) and 3-amino-3-methylbutanoic acid (700 mg) were dissolved in N,N-dimethylformamide (30 ml). N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (876 mg) and hydroxybenzotriazole (698 mg) were added thereto at 0° C., and then the mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, and water and ethyl acetate were added to the residue. The organic phase was separated, and the aqueous phase was adjusted to pH 9 by adding a saturated sodium bicarbonate solution, and then extracted with ethyl acetate. The extract was dried over sodium sulfate and concentrated under reduced pressure to give the title compound (0.60 g, Y.:60%) as a brown oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345180B2
Source datasetuspto-grants-2008_03
ORD IDord-5df6aa48d0714eeaaf4457e442735942
Source noteuspto-grants-2008_03