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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69371Generated: October 29, 2026

2-(4-((1-(5-Fluoro-2-methylphenyl)propan-2-yl)amino)-2-oxo-1,2-dihydropyridin-3-yl)-6-isopropylimidazo[4,5-f]isoindole-5,7(1H,6H)-dione → HCID 136340654, compound

https://huagongshe.com/reaction/69371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-((1-(5-Fluoro-2-methylphenyl)propan-2-yl)amino)-2-oxo-1,2-dihydropyridin-3-yl)-6-isopropylimidazo[4,5-f]isoindole-5,7(1H,6H)-dioneHCID 136340655—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
ProductHCID 136340654HCID 136340654—

Reaction Steps

2-(4-((1-(5-Fluoro-2-methylphenyl)propan-2-yl)amino)-2-oxo-1,2-dihydropyridin-3-yl)-6-isopropylimidazo[4,5-f]isoindole-5,7(1H,6H)-dione (0.138 g) and zinc powder (0.4 g) were suspended in acetic acid (10 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 an off-white solid product, 0.086 g. MS: 473.9 [M+1]. 1H NMR (DMSO-d6, 500 MHz): δ 13.06 (s, 1H), 11.15 (s, 1H), 11.01-11.00 (d, 1H), 7.95 (s, 0.5H), 7.84-7.82 (d, 0.5H), 7.70 (s, 0.5H), 7.30-7.10 (m, 3H), 6.91-6.84 (m, 1H), 6.15-6.11 (dd, 1H), 4.51-4.42 (m, 3H), 4.18-4.13 (m, 1H), 3.32 (s, 1H), 2.99-2.97 (m, 2H), 2.36 (d, 3H), 1.34 (d, 3H), 1.23 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822500B2
Source datasetuspto-grants-2014_09
ORD IDord-2866e58214334401b8adae61bcd35f13
Source noteuspto-grants-2014_09