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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022437Generated: October 30, 2026

1-(2-Fluorophenyl)piperazine → HCID 72548961, compound

https://huagongshe.com/reaction/1022437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Fluorophenyl)piperazineHCID 70529—
ReactantHCID 86704560HCID 86704560—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 72548961HCID 7254896165.3%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 6-chloro-1-ethyl-1,5-dihydro-pyrrolo[3,2-c]pyridine-4-one (Intermediate G) (16 mg, 0.081 mmol) and 1-(2-fluorophenyl)piperazine (160 mg, 0.888 mmol) was heated at 140° C. in a sealed tube for 5 h. Flash chromatography (20/1 methylene chloride/methanol) afforded 1-ethyl-6-[4-(2-fluoro-phenyl)-piperazin-1-yl]-1,5-dihydro-pyrrolo[3,2-c]pyridin-4-one (18 mg, 65%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.3 (t, J=7.28 Hz, 3H) 3.1 (d, J=4.77 Hz, 4H) 3.2 (d, J=4.77 Hz, 4H) 4.0 (q, J=7.19 Hz, 2H) 5.8 (s, 1H) 6.3 (d, J=3.01 Hz, 1H) 6.9 (d, J=3.01 Hz, 1H) 7.1-7.2 (m, 3H) 10.6 (s, 1H). LC-MS calcd. for C19H22FN4O [(M+H)+] 341, obsd. 341.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722661B2
Source datasetuspto-grants-2014_05
ORD IDord-18ca75c87f6c4ceb8131b5981bde3357
Source noteuspto-grants-2014_05