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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234885Generated: November 1, 2026

3-(5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(5-(3-methylphenyl)-1H-indol-3-yl)pyrrole-2,5-dione → HCID 86608192, compound

https://huagongshe.com/reaction/2234885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(5-(3-methylphenyl)-1H-indol-3-yl)pyrrole-2,5-dioneHCID 68494641—
SolventMethanolHCID 887—
ProductHCID 86608192HCID 86608192—

Reaction Steps

3-(5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1yl)-4-(5-(3-methylphenyl)-1H-indol-3-yl) pyrrole-2,5-dione, prepared as in Example 34, was reduced with Mg in methanol as described in Example 2, Procedure C, to yield (±)-trans-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1yl)-4-(5-(3-methylphenyl)-1H-indol-3-yl)pyrrolidine-2,5-dione. 1H NMR (CD3OD) δ: 1.98-2.18(m, 2H), 2.34(s, 3H), 2.85-3.00(m, 2H), 3.90-3.98(m, 1H), 3.98-4.09(m, 1H), 4.35(d, J=7.2 Hz, 1H), 4.64(d, J=6.8 Hz, 1H), 6.88-6.99(m, 2H), 7.00-7.10(m, 3H), 7.13-7.26(m, 5H), 7.36(m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713969B2
Source datasetuspto-grants-2010_05
ORD IDord-c1f5ba32034d4c30a29cd06fe80f5b9a
Source noteuspto-grants-2010_05