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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926709Generated: November 1, 2026

Dimethylcarbamoyl Chloride → (3S)-3-Amino-1-[(dimethylcarbamoyl)oxy]-6-phenoxy-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1926709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
ReactantHCID 131729734HCID 131729734—
SolventPyridineHCID 1049—
Product(3S)-3-Amino-1-[(dimethylcarbamoyl)oxy]-6-phenoxy-3,4-dihydroquinolin-2(1H)-oneHCID 5962715565%

Reaction Steps

Dimethylcarbamyl chloride (37 μL, 0.39 mmol) was added to a solution of (3S)-3-amino-1-hydroxy-6-phenoxy-3,4-dihydroquinolin-2(1H)-one, hydrochloride salt (93, Example 71) (100 mg, 0.33 mmol) in pyridine (2 mL). The reaction mixture was maintained at RT for 1.5 h, then concentrated in vacuo; the resulting residue was diluted with EtOAc (20 mL) and water (10 mL). The separated organic phase was washed with water (10 mL), dried over Mg2SO4, filtered, and concentrated in vacuo to provide the title compound as an oil (72 mg, 65%). LCMS m/z 253.0 [(M-dimethyl carbamic acid)+1]. 1H NMR (400 MHz, CD3OD) δ 2.94-3.02 (m, 1H), 3.02 (br s, 3H), 3.08 (dd, half of ABX pattern, J=15.5, 6.4 Hz, 1H), 3.17 (br s, 3H), 3.78 (dd, J=13.3, 6.3 Hz, 1H), 6.90-7.00 (m, 5H), 7.11 (ddt, J=7.7, 7.1, 1.1 Hz, 1H), 7.32-7.37 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183238B2
Source datasetuspto-grants-2012_05
ORD IDord-58a1f9fceabb466fb7e2d6639cd31627
Source noteuspto-grants-2012_05