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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970493Generated: October 29, 2026

2-Furancarbonyl chloride → 4-[4-(Furan-2-carbonyl)-piperazin-1-yl]-1,6-dimethyl-2-oxo-1,2-dihydro-quinolin-3-carbonitrile

https://huagongshe.com/reaction/970493

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furancarbonyl chlorideHCID 68242—
Reactant1,6-Dimethyl-2-oxo-4-piperazin-1-yl-1,2-dihydro-quinoline-3-carbonitrileHCID 21081901—
SolventPyridineHCID 1049—
Product4-[4-(Furan-2-carbonyl)-piperazin-1-yl]-1,6-dimethyl-2-oxo-1,2-dihydro-quinolin-3-carbonitrileHCID 2108195359%

Reaction Steps

2-Furoyl chloride (148 μL, 1.5 mmol) was added to a stirred solution of Compound 28 (282 mg, 1.0 mmol) in pyridine (5 mL) under argon at 0° C. The solution was allowed to come to room temperature and further stirred overnight. The solution was poured into ice water and the solids formed were filtered. The solids were washed by excess water, dried, and recrystallized by ethyl acetate to yield 221 mg (59%) of white solids. M.P. 231° C. 1H NMR (DMSO-d6): δ 2.41 (s, 3H), 3.56 (s, 3H), 3.63 (m, 4H), 3.95 (m, 4H), 6.66 (dd, J=1.5, 3.6 Hz, 1H), 7.08 (d, J=3.4 Hz, 1H), 7.48 (d, J=8.7 Hz, 1H), 7.59 (dd, J=1.2, 8.8 Hz, 1H), 7.69 (s, 1H), 7.88 (s, 1H). EIMS m/z 399 (M+23). Anal. (C21H20N4O3) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312220B2
Source datasetuspto-grants-2007_12
ORD IDord-c9a7a2b7d9184476b6744df8c20974b8
Source noteuspto-grants-2007_12