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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205671Generated: October 31, 2026

3-Bromo-1-methyl-1,2-dihydroquinolin-2-one → HCID 131735819, compound

https://huagongshe.com/reaction/2205671

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-1-methyl-1,2-dihydroquinolin-2-oneHCID 268315—
Reactanttert-Butyl (2-(methoxy(methyl)amino)-2-oxoethyl)carbamateHCID 4428209—
ReactantHCID 178418918HCID 178418918—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131735819HCID 131735819—

Reaction Steps

To a 0.3 M solution of 3-bromo-1-methylquinolin-2(1 H)-one (1 equiv; prepared as described in Tetrahedron, 64 (26), 6030-6037; 2008) and tert-butyl(2-(methoxy(methyl)amino)-2-oxoethyl)carbamate (1.2 eq) in dry THF, isopropylmagnesium chloride (3 eq) was added dropwise at room temperature. The mixture was stirred for 30 min at room temperature, diluted with dichloromethane, washed with sat. aq. NH4Cl dried (Na2SO4) and concentrated under reduced pressure. The residue was purified by flash chromatography (SiO2, Pethroleum ether/EtOAc, from 7% to 60% EtOAc). The pooled fractions were concentraded under vacuum to the title compound. MS (ES) C17H20N2O4 requires: 316.35, found: 317. 1H-NMR (400 MHz, DMSO-d6) δ: 8.53 (1 H, s), 7.99 (1 H, d, J=7.2 Hz), 7.78 (1 H, t, J=6.8 Hz), 7.61 (1 H, d, J=8.4 Hz), 7.35 (1 H, t, J=7.2 Hz), 6.97 (1 H, bt, J=5.6 Hz), 4.45 (1 H, d, J=5.6 Hz), 3.70 (3 H, s), 1.39 (9 H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371295B2
Source datasetuspto-grants-2016_06
ORD IDord-9acd58db10164f208a3877e76c4f4152
Source noteuspto-grants-2016_06