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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isoindoline | HCID 422478 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 3-Amino-3-methylbutanoic acid | HCID 2760933 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Amino-1-(1,3-dihydroisoindol-2-yl)-3-methylbutan-1-one | HCID 11535878 | 60.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07345180B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-5df6aa48d0714eeaaf4457e442735942 |
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| Source note | uspto-grants-2008_03 |
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