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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247522Generated: October 25, 2026

Sodium hydride → 3-Amino-1-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1247522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-Amino-3,4-dihydroquinolin-2(1H)-one--hydrogen chloride (1/1)HCID 13499428—
Reactant(2,2-Dimethyl-1,3-dioxolan-4-yl)methyl methanesulfonateHCID 15570840—
SolventDimethylformamideHCID 6228—
Product3-Amino-1-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-3,4-dihydroquinolin-2(1H)-oneHCID 2190682153%

Reaction Conditions

Temperature80 °C

Reaction Steps

Sodium hydride (60% in oil, 191 mg, 4.70 mmol) was added to 3-amino-3,4-dihydroquinolin-2(1H)-one hydrochloride (J. Med. Chem., 28, 1985; 1511–16,450 mg, 2.27 mmol), in anhydrous DMF (6 mL) at 0° C. over a period of 5 min keeping the internal temperature at <10° C. The reaction was stirred for a further 30 min before addition of (2,2-dimethyl-1,3-dioxolan-4-yl)methyl methanesulfonate (J. Med. Chem. 35, 1992, 1650–62; 528 mg, 2.50 mmol) and the reaction has then heated to 80° C. for a period of 5 h. The reaction was then cooled and evaporated before addition of sat. aqueous NaHCO3 (20 mL) and EtOAc (50 mL). The organic layer was then dried (MgSO4), filtered and evaporated and the residue was purified by column chromatography (MeOH:DCM 1:19) to afford the title compound (330 mg, 53%) as colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129249B2
Source datasetuspto-grants-2006_10
ORD IDord-c9898cd3b4694b7ca5f894223eb35679
Source noteuspto-grants-2006_10