HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409486Generated: October 29, 2026
Diisopropylethylamine → HCID 178425377, compound
https://huagongshe.com/reaction/2409486
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86677133 | HCID 86677133 | — |
| Reactant | HCID 178514857 | HCID 178514857 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178425377 | HCID 178425377 | 59.7% |
Reaction Steps
A solution of 2-(4-chloro-2-oxo-1,2-dihydropyridin-3-yl)-6-(2-pyrrolidin-1-ylethyl)-6,7-dihydroimidazo[4,5-f]isoindol-5(3H)-one (50 mg, 0.126 mmol), (1S)-2-(5-chloro-2-methylphenyl)-1-methylethylamine (30 mg, 0.164 mmol) and DIEA (66 uL, 0.38 mmol) in 2 mL of EtOH was heated at 80° C. for 24 h. Then the solvent was evaporated and the residue was purified by column (silica gel, DCM:MeOH 95:5) to give 2-(4-((1S)-2-(5-cloro-2-methylphenyl)-1-methylethylamino)-2-oxo-1,2-dihydropyridin-3-yl)-6-(2-pyrrolidin-1-ylethyl)-6,7-dihydroimidazo[4,5-f]isoindol-5(3H)-one (41 mg, 59%) as yellow solid. ESI-MS: m/z (MH+) 545.5. 1H NMR (300 MHz, CDCl3): δ 7.96 (d, J=44.8 Hz, 1H), 7.51 (d, J=66.3 Hz, 1H), 7.20 (m, 2H), 7.03 (m, 2H), 5.86 (m, 1H), 4.59 (m, 2H), 3.93 (m, 3H), 2.96-3.13 (m, 8H), 2.32 (s, 3H), 1.91 (m, 4H), 1.38 (d, J=7.35 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815906B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-f7048c1fd67c4001a84542900decb3d0 |
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| Source note | uspto-grants-2014_08 |
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