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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405898Generated: October 30, 2026

(+/-)-trans-3-[4-(benzyloxy)phenyl]-4-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)pyrrolidine-2,5-dione → (+/-)-trans-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(4-hydroxyphenyl)pyrrolidine-2,5-dione

https://huagongshe.com/reaction/405898

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-trans-3-[4-(benzyloxy)phenyl]-4-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)pyrrolidine-2,5-dioneHCID 69396599—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Product(+/-)-trans-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(4-hydroxyphenyl)pyrrolidine-2,5-dioneHCID 6939759344.1%

Reaction Steps

A mixture of (±)-trans-3-[4-(benzyloxy)phenyl]-4-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)pyrrolidine-2,5-dione (0.2 g) and Pd/C (10% w/w, 0.076 g) was stirred under 1 atmosphere of hydrogen gas overnight. The catalyst was filtered off through a pad of celite and concentrated. The residue was purified by column chromatography on silica gel eluting with 30-40% ethyl acetate in hexane to provide (±)-trans-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(4-hydroxyphenyl)pyrrolidine-2,5-dione 0.07 g as a light yellow solid. Mp 105-107° C.; 1H NMR (acetone-d6) 400 MHz δ: 10.27 (s. 1 H), 8.34 (s, 1 H), 7.17-7.21 (m, 4 H), 6.80-6.91 (m, 4 H), 4.39 (d, J=7.0 Hz, 1 H), 4.22 (d, J=7.0 Hz, 1 H), 4.13 (d, J=5.6 Hz, 2 H), 2.92 (d, J=5.2 Hz, 2 H), 2.15-2.19 (m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754078B2
Source datasetuspto-grants-2014_06
ORD IDord-d8db5065dc80417e8b48f52859f86b24
Source noteuspto-grants-2014_06