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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103205Generated: October 29, 2026

Sodium hydride → 1-(3-Chloropropyl)-6,7-difluoro-3,4-dihydro-1H-quinolin-2-one

https://huagongshe.com/reaction/2103205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Chloro-3-iodopropaneHCID 81363—
Reactant6,7-Difluoro-3,4-dihydroquinolin-2(1h)-oneHCID 14853334—
SolventDimethylformamideHCID 6228—
Product1-(3-Chloropropyl)-6,7-difluoro-3,4-dihydro-1H-quinolin-2-oneHCID 1795616947.5%

Reaction Steps

A reaction flask was charged with 6,7-difluoro-3,4-dihydro-1H-quinolin-2-one (97KK47) (0.181 g, 0.99 mmol) in dry DMF (5 mL) under an argon atmosphere. Washed NaH (0.026 g, 1.08 mmol) was added and the mixture was stirred at rt for 0.5 h. Then 3-chloro-1-iodopropane (0.205 g, 1.00 mmol) dissolved in DMF (1 mL) was added followed by stirring at rt for 20 h. The reaction mixture was quenched with water, and the product extracted into Et2O. The combined organic layers were washed with aqueous 4% MgSO4, dried over Na2SO4, filtered, and concentrated. The product was purified by flash CC (SiO2; DCM) to give the title compound (112KK03) (0.122 g, 47%). 1H NMR (CD3OD) δ 6.99-6.86 (m, 2H), 4.03-3.99 (m, 2H), 3.60 (t, J=6.1, CH2), 2.84-2.81 (m, 2H), 2.63-2.59 (m, 2H), 2.13-2.06 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576100B2
Source datasetuspto-grants-2009_08
ORD IDord-0bc18bc403d24c56a64f9275706aafb0
Source noteuspto-grants-2009_08