HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920473Generated: October 31, 2026
(S)-2-(2-oxo-4-((1-(2,3,5,6-tetrafluorophenyl)propan-2-yl)amino)-1,2-dihydropyridin-3-yl)-6-(pyridin-3-yl)imidazo[4,5-f]isoindole-5,7(1H,6H)-dione → HCID 136353611, compound
https://huagongshe.com/reaction/920473
Participants
| Role | Name | HCID | Charge |
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| Reactant | (S)-2-(2-oxo-4-((1-(2,3,5,6-tetrafluorophenyl)propan-2-yl)amino)-1,2-dihydropyridin-3-yl)-6-(pyridin-3-yl)imidazo[4,5-f]isoindole-5,7(1H,6H)-dione | HCID 136353563 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 136353611 | HCID 136353611 | 32.6% |
Reaction Steps
Compound (S)-2-(2-oxo-4-((1-(2,3,5,6-tetrafluorophenyl)propan-2-yl)amino)-1,2-dihydropyridin-3-yl)-6-(pyridin-3-yl)imidazo[4,5-f]isoindole-5,7(1H,6H)-dione (0.46 g, 0.82 mmol) and zinc powder (1.23 g, 18.8 mmol) were suspended in acetic acid (30 mL). The reaction mixture was stirred and heated to reflux overnight under argon. Then, the solvent was removed under reduced pressure. The residue solid was stirred in 50 mL of saturated K2CO3 solution. The white solid was filtered out, dried under vacuum and extracted with CH2Cl2/MeOH (7/3 v/v) three times (150 mL). The extracts were concentrated to dryness. The residue was purified by column chromatography (silica-gel, CH2Cl2/MeOH=9/1 v/v) to give a white solid product, 0.15 g, 32.6% yield. MS: 563.0 [M−H]−. 1H NMR (DMSO-d6, 500 MHz): δ 13.21-13.19 (m, 1H), 11.30-11.29 (m, 1H), 11.13-11.09 (m, 1H), 9.08 (s, 1H), 8.41 (d, 1H, J=3.5 Hz), 8.26 (d, 1H, J=7.0 Hz), 8.11 (s, 0.5H), 7.98 (s, 0.5H), 7.90 (s, 0.5 Hz), 7.78-7.73 (m, 1.5H), 7.52-7.50 (m, 1H), 7.41-7.38 (m, 1H), 6.93-6.90 (m, 1H), 6.67-6.64 (m, 1H), 6.20-6.17 (m, 1H), 4.26-4.25 (m, 1H), 3.19-3.14 (m, 2H), 1.41 (d, 3H, J=5.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273055B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-e2e99040d1b74e58aa4e9087405392ee |
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| Source note | uspto-grants-2016_03 |
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