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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromo-1-methyl-1,2-dihydroquinolin-2-one | HCID 268315 | — |
| Reactant | tert-Butyl (2-(methoxy(methyl)amino)-2-oxoethyl)carbamate | HCID 4428209 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131735819 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371295B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-9acd58db10164f208a3877e76c4f4152 |
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| Source note | uspto-grants-2016_06 |
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