HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718717Generated: November 1, 2026
3-Aminophthalic acid → 4-amino-2-(2-oxopiperidin-3-yl)-2,3-dihydro-1H-isoindole-1,3-dione
https://huagongshe.com/reaction/718717
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminophthalic acid | HCID 79490 | — |
| Reactant | 3-Amino-2-piperidone | HCID 5200225 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-amino-2-(2-oxopiperidin-3-yl)-2,3-dihydro-1H-isoindole-1,3-dione | HCID 58572147 | 35% |
Reaction Steps
To a solution of 3-aminophthalic acid (0.100 g, 0.552 mmol) in DMF (1.1 mL) was added 3-aminopiperidine-2-one (0.063 g, 0.552 mmol) and the reaction was stirred at 90° C. over 18 h. Volatiles were removed in vacuo and the dark-brown crude residue was purified by preparative reverse phase HPLC to give the desired product 28 (0.050 g, 35%) as an off-white powder. 1H NMR (400 MHz, DMSO) δ 7.83 (s, 1H), 7.43 (dd, J=8.3, 7.1 Hz, 1H), 7.07-6.87 (m, 2H), 6.47 (br s, 2H), 4.49 (dd, J=11.9, 6.3 Hz, 1H), 3.27-3.10 (m, 2H), 2.19 (dt, J=12.0, 7.7 Hz, 1H), 2.05-1.72 (m, 3H). MS (ESI) m/z calcd for C13H14N3O3 [M+H]+ 260.3, found: 260.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193989B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-049fff498c564f37b6548b05bb0d0ab3 |
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| Source note | uspto-grants-2015_11 |
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