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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920508Generated: October 30, 2026

2-(4-(1-(2,3,5,6-Tetrafluorophenyl)propan-2-ylamino)-2-oxo-1,2-dihydropyridin-3-yl)-6-methylimidazo[4,5-f]isoindole-5,7(1H,6H)-dione → HCID 136340662, compound

https://huagongshe.com/reaction/920508

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(1-(2,3,5,6-Tetrafluorophenyl)propan-2-ylamino)-2-oxo-1,2-dihydropyridin-3-yl)-6-methylimidazo[4,5-f]isoindole-5,7(1H,6H)-dioneHCID 136340661—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
ProductHCID 136340662HCID 13634066262.6%

Reaction Steps

2-(4-(1-(2,3,5,6-Tetrafluorophenyl)propan-2-ylamino)-2-oxo-1,2-dihydropyridin-3-yl)-6-methylimidazo[4,5-f]isoindole-5,7(1H,6H)-dione (0.51 g, 1.02 mmol) and zinc powder (1.60 g, 24.51 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 100 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 (300 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 pale-yellow solid product, 0.31 g, 62.6% yield. MS: 508.0 [M+Na]+. 1H NMR (DMSO-d6, 500 MHz): δ 13.03 (s, 1H), 11.24 (s, 1H), 11.14-11.11 (m, 1H), 7.95 (s, 0.5H), 7.78-7.74 (m, 2H), 7.61 (s, 0.5H), 7.35 (s, 1H), 6.15 (s, 1H), 4.48 (s, 2H), 4.22 (m, 1H), 3.17-3.10 (m, 2H), 3.09 (s, 3H), 1.37 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273055B2
Source datasetuspto-grants-2016_03
ORD IDord-ae871d7756aa4e819d73ee9011a4f032
Source noteuspto-grants-2016_03