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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376157Generated: October 31, 2026

Sodium hydride → 3-amino-1-[(2,2-dimethyl-1,3-dioxan-5-yl)methyl]-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1376157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(2,2-Dimethyl-1,3-dioxan-5-yl)methyl methanesulfonateHCID 10998661—
Reactant3-Amino-3,4-dihydroquinolin-2(1H)-one--hydrogen chloride (1/1)HCID 13499428—
SolventDimethylformamideHCID 6228—
Product3-amino-1-[(2,2-dimethyl-1,3-dioxan-5-yl)methyl]-3,4-dihydroquinolin-2(1H)-oneHCID 2190683057.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium hydride (60% in oil, 1.60 g, 39.80 mmol) was added to 3-amino-3,4-dihydroquinolin-2(1H)-one hydrochloride (3.59 g, 18.09 mmol), in anhydrous DMF (50 mL) at 0° C. over a period of 10 min. The reaction was stirred for a further 30 min before addition of (2,2-dimethyl-1,3-dioxan-5-yl)methyl methanesulfonate [CAS registary number 131372-64-0] (4.05 g, 18.09 mmol) and the reaction has then heated to 60° C. for a period of 16 h. The reaction was then cooled and evaporated before addition of sat. aqueous NaHCO3 (200 mL) and EtOAc (500 mL). The organic layer was then dried (MgSO4), filtered and evaporated and the residue was purified by column chromatography (MeOH:DCM, 3:37) to afford the title compound (3.00 g, 57%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169927B2
Source datasetuspto-grants-2007_01
ORD IDord-ed493a177eb04dc0859eda4ebdbf598d
Source noteuspto-grants-2007_01