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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234890Generated: October 25, 2026

2-(Thiophen-3-yl)acetamide → (+/-)-Trans-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(thiophen-3-yl) pyrrolidine-2,5-dione

https://huagongshe.com/reaction/2234890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Thiophen-3-yl)acetamideHCID 566335—
Reactant2-(2-Chloro-4-fluorophenyl)acetamideHCID 2773716—
Product(+/-)-Trans-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4-(thiophen-3-yl) pyrrolidine-2,5-dioneHCID 86608197—

Reaction Steps

(±)-Trans-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1yl)-4-(thiophen-3-yl)pyrrolidine-2,5-dione was prepared according to Example 40 replacing 2-chloro-4-fluorophenylacetamide with thiophen-3-ylacetamide. Yield 50.3 mg, 15.0%. 1H NMR (DMSO-d6) 400 MHz δ: 11.50 (s, 1H), 7.52 (m, 1H), 7.49 (m, 1H), 7.35 (s, 1H), 7.21 (dd, 1H, J=4.01.2 Hz), 7.16 (d, 1H, 7.6 Hz), 6.89 (d, 1H, J=4.4 Hz), 6.85 (t, 1H, J=6.8 Hz), 4.56 (d, 1H, J=7.2 Hz), 4.41 (d, 1H, J=7.2 Hz), 4.10 (t, 2H, J=6.0 Hz), 2.90 (t, 2H, J=6.0 Hz), 2.10 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713969B2
Source datasetuspto-grants-2010_05
ORD IDord-d1bc6c282c1a4afebab54c9bbf22d647
Source noteuspto-grants-2010_05